Variant report

Variant	esv1792828
Chromosome Location	chr17:57185807-57219391
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:232)
CpG islands
(count:184)
Chromatin interactive
region (count:105)
LncRNA
region (count:1)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:232 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr17:57202027-57202375	GM12878	blood:	n/a	n/a
2	BATF	chr17:57190737-57190906	GM12878	blood:	n/a	n/a
3	BATF	chr17:57201997-57202383	GM12878	blood:	n/a	n/a
4	BCL11A	chr17:57202069-57202310	GM12878	blood:	n/a	n/a
5	BCL11A	chr17:57190732-57190901	GM12878	blood:	n/a	n/a
6	BRCA1	chr17:57190814-57190841	GM12878	blood:	n/a	n/a
7	CEBPB	chr17:57215608-57216113	MCF-7	breast:	n/a	n/a
8	CEBPB	chr17:57212605-57212764	IMR90	lung:	n/a	chr17:57212648-57212659
9	CEBPB	chr17:57215709-57215972	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr17:57215774-57215971	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr17:57215776-57215956	K562	blood:	n/a	n/a
12	CEBPB	chr17:57212552-57212785	HepG2	liver:	n/a	chr17:57212648-57212659
13	CEBPB	chr17:57215770-57215969	A549	lung:	n/a	n/a
14	CEBPB	chr17:57215764-57215957	IMR90	lung:	n/a	n/a
15	CEBPB	chr17:57215782-57215980	HepG2	liver:	n/a	n/a
16	CREB1	chr17:57202035-57202404	GM12878	blood:	n/a	n/a
17	CTCF	chr17:57190805-57190921	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr17:57190824-57190880	GM12892	blood:	n/a	n/a
19	CTCF	chr17:57190811-57190893	A549	lung:	n/a	n/a
20	CTCF	chr17:57196600-57196750	MCF-7	breast:	n/a	n/a
21	CTCF	chr17:57190803-57190914	GM12891	blood:	n/a	n/a
22	CTCF	chr17:57217860-57218010	A549	lung:	n/a	n/a
23	CTCF	chr17:57190720-57190870	GM12873	blood:	n/a	n/a
24	CTCF	chr17:57186500-57186650	MCF-7	breast:	n/a	n/a
25	CTCF	chr17:57185760-57185910	MCF-7	breast:	n/a	n/a
26	CTCF	chr17:57190766-57190943	ProgFib	skin:	n/a	n/a
27	CTCF	chr17:57199280-57199430	MCF-7	breast:	n/a	n/a
28	CTCF	chr17:57190760-57190910	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr17:57195680-57195830	MCF-7	breast:	n/a	n/a
30	CTCF	chr17:57218448-57218510	Lung_OC	lung:	n/a	n/a
31	CTCF	chr17:57199600-57199750	MCF-7	breast:	n/a	n/a
32	CTCF	chr17:57194880-57195030	MCF-7	breast:	n/a	n/a
33	CTCF	chr17:57190808-57190904	Fibrobl	skin:	n/a	n/a
34	CTCF	chr17:57192860-57193010	MCF-7	breast:	n/a	n/a
35	CTCF	chr17:57190852-57190880	Gliobla	brain:	n/a	n/a
36	CTCF	chr17:57188960-57189110	MCF-7	breast:	n/a	n/a
37	CTCF	chr17:57190811-57190895	GM19238	blood:	n/a	n/a
38	CTCF	chr17:57191380-57191530	MCF-7	breast:	n/a	n/a
39	CTCF	chr17:57190825-57190848	Gliobla	brain:	n/a	n/a
40	CTCF	chr17:57213746-57213799	GM13976	blood:	n/a	n/a
41	EBF1	chr17:57190738-57190909	GM12878	blood:	n/a	n/a
42	EBF1	chr17:57199515-57199762	GM12878	blood:	n/a	n/a
43	ELK1	chr17:57190814-57190845	GM12878	blood:	n/a	n/a
44	EP300	chr17:57190718-57190960	GM12878	blood:	n/a	n/a
45	EP300	chr17:57190746-57190898	GM12878	blood:	n/a	n/a
46	FOS	chr17:57199601-57199801	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr17:57199659-57199806	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr17:57217412-57217471	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr17:57217410-57217543	MCF10A-Er-Src	breast:	n/a	n/a
50	FOSL2	chr17:57199215-57199835	MCF-7	breast:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:57216476-57216526	K562	blood:	n/a
2	chr17:57216476-57216526	K562	blood:	n/a
3	chr17:57187728-57187778	ovcar-3	ovarian:	n/a
4	chr17:57187728-57187778	NB4	blood:	n/a
5	chr17:57187728-57187778	HIPEpiC	eye:	n/a
6	chr17:57216476-57216526	MCF10A-Er-Src	breast:	n/a
7	chr17:57187728-57187778	BE2_C	brain:	n/a
8	chr17:57187728-57187778	PANC-1	pancreas:	n/a
9	chr17:57216484-57216534	AG10803	skin:	n/a
10	chr17:57187728-57187778	AoSMC	blood vessel:	n/a
11	chr17:57187728-57187778	MCF-7	breast:	n/a
12	chr17:57216484-57216534	Hepatocyte	liver:	n/a
13	chr17:57187728-57187778	HCM	heart:	n/a
14	chr17:57187728-57187778	HAEpiC	amniotic membrane:	n/a
15	chr17:57216484-57216534	HPAEpiC	pulmonary alveolar:	n/a
16	chr17:57216476-57216526	AoSMC	blood vessel:	n/a
17	chr17:57187728-57187778	AG09319	gingival:	n/a
18	chr17:57216484-57216534	AG04449	skin:	fetal
19	chr17:57216476-57216526	HNPCEpiC	eye:	n/a
20	chr17:57216484-57216534	H1-hESC	embryonic stem cell:	embryo
21	chr17:57216484-57216534	GM06990	blood:	n/a
22	chr17:57216484-57216534	U87	brain:	n/a
23	chr17:57216484-57216534	HUVEC	blood vessel:	n/a
24	chr17:57187728-57187778	AG10803	skin:	n/a
25	chr17:57216476-57216526	ECC-1	luminal epithelium:	n/a
26	chr17:57216484-57216534	HCM	heart:	n/a
27	chr17:57187728-57187778	AG04449	skin:	fetal
28	chr17:57216484-57216534	HMEC	breast:	n/a
29	chr17:57216476-57216526	BE2_C	brain:	n/a
30	chr17:57216476-57216526	AG10803	skin:	n/a
31	chr17:57216476-57216526	H1-hESC	embryonic stem cell:	embryo
32	chr17:57216476-57216526	T-47D	breast:	n/a
33	chr17:57216476-57216526	HCT-116	colon:	n/a
34	chr17:57216476-57216526	GM12892	blood:	n/a
35	chr17:57216476-57216526	NHBE	bronchial:	n/a
36	chr17:57187728-57187778	NHBE	bronchial:	n/a
37	chr17:57187728-57187778	HepG2	liver:	n/a
38	chr17:57187728-57187778	HEK293	kidney:	embryo
39	chr17:57187728-57187778	T-47D	breast:	n/a
40	chr17:57216476-57216526	PANC-1	pancreas:	n/a
41	chr17:57187728-57187778	PFSK-1	brain:	n/a
42	chr17:57216484-57216534	BJ	skin:	n/a
43	chr17:57216484-57216534	AG09309	skin:	n/a
44	chr17:57216484-57216534	PANC-1	pancreas:	n/a
45	chr17:57216484-57216534	SK-N-SH_RA	brain:	n/a
46	chr17:57187728-57187778	SK-N-SH_RA	brain:	n/a
47	chr17:57187728-57187778	HCF	heart:	n/a
48	chr17:57216484-57216534	LNCaP	prostate:	n/a
49	chr17:57187728-57187778	HPAEpiC	pulmonary alveolar:	n/a
50	chr17:57216484-57216534	PrEC	prostate:	n/a

(count:105 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr17:56755909..56758156-chr17:57194925..57196725,2	K562	blood:
2	chr17:57181740..57185864-chr17:57285843..57288823,5	K562	blood:
3	chr17:57209257..57211586-chr17:57216114..57217876,2	K562	blood:
4	chr17:57213191..57215400-chr17:57226775..57229710,2	MCF-7	breast:
5	chr17:18160519..18163064-chr17:57184178..57185847,2	MCF-7	breast:
6	chr17:57194795..57197168-chr17:57199676..57202455,3	K562	blood:
7	chr17:57211313..57212962-chr17:57215740..57218638,2	MCF-7	breast:
8	chr17:57215551..57217180-chr17:57231938..57233517,2	MCF-7	breast:
9	chr17:57198627..57199337-chr17:57908770..57909736,2	MCF-7	breast:
10	chr17:57188404..57190488-chr17:57204036..57205659,2	MCF-7	breast:
11	chr17:57201244..57203601-chr17:57231606..57233298,2	K562	blood:
12	chr17:57186315..57188698-chr17:57208953..57211080,2	MCF-7	breast:
13	chr17:57194795..57197168-chr17:57199676..57202455,3	K562	blood:
14	chr17:57182396..57186542-chr17:57229642..57234395,10	MCF-7	breast:
15	chr17:57192158..57194327-chr17:57196141..57198437,2	K562	blood:
16	chr17:57211421..57213202-chr17:57224017..57226247,2	K562	blood:
17	chr17:57182042..57184232-chr17:57211230..57213577,2	MCF-7	breast:
18	chr17:57189365..57191932-chr3:39147669..39149777,2	MCF-7	breast:
19	chr17:57187733..57190486-chr17:57190590..57192195,2	K562	blood:
20	chr17:56706387..56711193-chr17:57182654..57188385,13	MCF-7	breast:
21	chr17:57193455..57195222-chr17:57217534..57219238,2	K562	blood:
22	chr17:56734902..56736637-chr17:57196658..57198160,2	MCF-7	breast:
23	chr17:56736795..56739319-chr17:57201589..57204473,2	MCF-7	breast:
24	chr17:57215736..57218282-chr17:57221813..57223603,3	K562	blood:
25	chr17:57190476..57192920-chr6:30583044..30584685,2	MCF-7	breast:
26	chr17:57195215..57197252-chr2:166649184..166651659,2	MCF-7	breast:
27	chr17:57191560..57194513-chr17:57208334..57210650,2	K562	blood:
28	chr17:57216218..57217783-chr17:57218957..57221471,2	K562	blood:
29	chr17:57182638..57185887-chr17:57231156..57234780,6	K562	blood:
30	chr17:56755806..56758382-chr17:57185281..57187565,2	K562	blood:
31	chr17:57187733..57190486-chr17:57190590..57192195,2	K562	blood:
32	chr17:57188404..57190488-chr17:57204036..57205659,2	MCF-7	breast:
33	chr17:57183248..57185852-chr17:57209111..57211158,2	MCF-7	breast:
34	chr17:57206910..57209463-chr17:57231955..57233663,2	MCF-7	breast:
35	chr17:57195175..57198107-chr17:57227392..57229706,3	K562	blood:
36	chr17:57196679..57198577-chr9:33164866..33167555,2	MCF-7	breast:
37	chr1:234744816..234747608-chr17:57184525..57186188,2	MCF-7	breast:
38	chr1:160990813..160992339-chr17:57183553..57186254,2	MCF-7	breast:
39	chr17:57181898..57185943-chr17:57190637..57193896,5	K562	blood:
40	chr17:56734867..56737611-chr17:57184859..57187520,2	K562	blood:
41	chr17:57186315..57188698-chr17:57208953..57211080,2	MCF-7	breast:
42	chr17:57200028..57201874-chr17:57209514..57212226,2	MCF-7	breast:
43	chr17:57184547..57186791-chr17:59477596..59480419,4	MCF-7	breast:
44	chr17:57183920..57185873-chr20:52209285..52211377,2	MCF-7	breast:
45	chr17:57195368..57199396-chr17:57968669..57972101,6	MCF-7	breast:
46	chr17:57180707..57182986-chr17:57216885..57219479,2	MCF-7	breast:
47	chr17:57217370..57219452-chr17:57230547..57233288,2	K562	blood:
48	chr17:57212572..57215112-chr17:57232344..57234452,2	MCF-7	breast:
49	chr17:57209257..57211586-chr17:57216114..57217876,2	K562	blood:
50	chr17:56709170..56711385-chr17:57193700..57195670,2	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR11-1	chr17:57195285-57195628	ENSG00000224738.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-454-3p	chr17:57215148-57215170	MIMAT0003885
hsa-miR-454-5p	chr17:57215189-57215210	MIMAT0003884

No data

Variant related genes	Relation type
RNU2-58P	TF binding region
TRIM37	TF binding region
MIR454	TF binding region
RNU2-58P	CpG island
TRIM37	CpG island
MIR454	CpG island
ENSG00000262251	chromatin interactions
ENSG00000200997	chromatin interactions
ENSG00000182628	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000167447	chromatin interactions
ENSG00000221299	chromatin interactions
ENSG00000207996	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000108389	chromatin interactions
ENSG00000266826	chromatin interactions
ENSG00000235192	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000172845	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000086062	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000168264	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000141510	chromatin interactions
ENSG00000115339	chromatin interactions
ENSG00000233554	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000252212	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000141499	chromatin interactions
ENSG00000201524	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000264672	chromatin interactions
ENSG00000177731	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000068489	chromatin interactions
ENSG00000158769	chromatin interactions
ENSG00000108395	chromatin interactions
ENSG00000224738	chromatin interactions
ENSG00000114745	chromatin interactions
ENSG00000168026	chromatin interactions
ENSG00000228393	chromatin interactions
SIK3	Mature miRNA region
MINPP1	Mature miRNA region
MRPS35	Mature miRNA region
UBR7	Mature miRNA region
BAHCC1	Mature miRNA region
IL5	Mature miRNA region
CSPP1	Mature miRNA region
MED12	Mature miRNA region
PPP1R7	Mature miRNA region
RPL4	Mature miRNA region
METTL2A	Mature miRNA region
PHF12	Mature miRNA region
MRPL37	Mature miRNA region
LTN1	Mature miRNA region
CHD7	Mature miRNA region
LRRC8D	Mature miRNA region
PRKCSH	Mature miRNA region
HMGXB3	Mature miRNA region
TET1	Mature miRNA region
TP53	Mature miRNA region
STK38	Mature miRNA region
ZNF805	Mature miRNA region
RAP2C	Mature miRNA region
SMAD4	Mature miRNA region
GID4	Mature miRNA region
POLR2A	Mature miRNA region
POFUT2	Mature miRNA region
TNKS2	Mature miRNA region
SPTSSA	Mature miRNA region
CEP152	Mature miRNA region
FLNC	Mature miRNA region
BHLHE40	Mature miRNA region
PCSK6	Mature miRNA region
ZBTB4	Mature miRNA region
USP25	Mature miRNA region
KCTD12	Mature miRNA region
C6orf120	Mature miRNA region
CNOT1	Mature miRNA region

Extended variants
information (count: 1056 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1056 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8082544	chr17:57185807-57185808	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146202401	chr17:57185815-57185816	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
3	rs545883569	chr17:57185837-57185838	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
4	rs35433470	chr17:57185867-57185868	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
5	rs557841469	chr17:57185954-57185955	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
6	rs571529290	chr17:57186000-57186001	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
7	rs114844088	chr17:57186036-57186037	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
8	rs139182852	chr17:57186061-57186062	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
9	rs529162533	chr17:57186084-57186085	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
10	rs541381674	chr17:57186119-57186120	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
11	rs538412483	chr17:57186126-57186127	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
12	rs559575119	chr17:57186205-57186206	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
13	rs533168567	chr17:57186233-57186234	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
14	rs551449031	chr17:57186281-57186282	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
15	rs565581421	chr17:57186295-57186296	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
16	rs576880205	chr17:57186371-57186372	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
17	rs569754994	chr17:57186397-57186398	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
18	rs189399564	chr17:57186416-57186417	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
19	rs536330566	chr17:57186430-57186431	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
20	rs116769167	chr17:57186456-57186457	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
21	rs553572971	chr17:57186544-57186545	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
22	rs144014159	chr17:57186670-57186671	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
23	rs536144752	chr17:57186718-57186719	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
24	rs547725783	chr17:57186744-57186745	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
25	rs565895243	chr17:57186784-57186785	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
26	rs200703829	chr17:57186824-57186825	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
27	rs576102859	chr17:57186832-57186833	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs61092888	chr17:57186833-57186834	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
29	rs367674594	chr17:57186835-57186836	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
30	rs397743110	chr17:57186842-57186843	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
31	rs28521339	chr17:57186843-57186844	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
32	rs28397793	chr17:57186844-57186845	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
33	rs28709281	chr17:57186851-57186852	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
34	rs28667831	chr17:57186860-57186861	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
35	rs368997553	chr17:57186867-57186868	Weak transcription Strong transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
36	rs75830468	chr17:57186872-57186873	Weak transcription Strong transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs76638415	chr17:57186874-57186875	Weak transcription Strong transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs576499472	chr17:57186903-57186904	Weak transcription Strong transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs146420555	chr17:57186919-57186920	Weak transcription Strong transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs182236285	chr17:57186979-57186980	Weak transcription Strong transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs186356056	chr17:57186980-57186981	Weak transcription Strong transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs190709101	chr17:57186996-57186997	Weak transcription Strong transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs577882386	chr17:57186998-57186999	Weak transcription Strong transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs576722357	chr17:57187001-57187002	Weak transcription Strong transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs545239166	chr17:57187002-57187003	Weak transcription Strong transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs563371378	chr17:57187099-57187100	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
47	rs530606723	chr17:57187217-57187218	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
48	rs371116921	chr17:57187346-57187347	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
49	rs548851465	chr17:57187481-57187482	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs182874831	chr17:57187482-57187483	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Neuroblastoma	18923191	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
Chordoma	18071362	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	21523713	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	19602461	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
small cell lung cancer	20016488	CNVD
Heart disease	20206336	CNVD
Limb Abnormalities	20206336	CNVD
Breast cancer	21467264	CNVD
Ovarian neoplasms	16753589	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Malignant melanoma	17260012	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16608533	CNVD
Lung cancer	18438408	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD

Chromatin state (count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:57183200-57186000	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr17:57183400-57186000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr17:57184600-57186600	Flanking Active TSS	Dnd41	blood
4	chr17:57184800-57190400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr17:57184800-57203200	Weak transcription	Gastric	stomach
6	chr17:57184800-57209000	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr17:57184800-57231000	Weak transcription	Aorta	Aorta
8	chr17:57185000-57186000	Enhancers	Brain Anterior Caudate	brain
9	chr17:57185000-57186000	Enhancers	Brain Substantia Nigra	brain
10	chr17:57185000-57186000	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr17:57185000-57186200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr17:57185000-57186200	Active TSS	GM12878-XiMat	blood
13	chr17:57185000-57188400	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr17:57185000-57188400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr17:57185000-57188400	Weak transcription	Placenta	Placenta
16	chr17:57185000-57188600	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr17:57185000-57188800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr17:57185000-57189000	Weak transcription	Fetal Kidney	kidney
19	chr17:57185000-57190200	Weak transcription	Fetal Muscle Leg	muscle
20	chr17:57185000-57190400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr17:57185000-57190400	Weak transcription	Left Ventricle	heart
22	chr17:57185000-57190400	Weak transcription	Thymus	Thymus
23	chr17:57185000-57190600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr17:57185000-57190600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr17:57185000-57190600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr17:57185000-57190800	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr17:57185000-57191200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr17:57185000-57191200	Weak transcription	Fetal Muscle Trunk	muscle
29	chr17:57185000-57191400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr17:57185000-57192400	Weak transcription	Right Atrium	heart
31	chr17:57185000-57194800	Weak transcription	HSMM	muscle
32	chr17:57185000-57196000	Weak transcription	Primary B cells from peripheral blood	blood
33	chr17:57185000-57198000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr17:57185000-57198200	Weak transcription	Spleen	Spleen
35	chr17:57185000-57199600	Weak transcription	Esophagus	oesophagus
36	chr17:57185000-57200600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr17:57185000-57203800	Weak transcription	Stomach Mucosa	stomach
38	chr17:57185000-57204600	Weak transcription	Ovary	ovary
39	chr17:57185000-57205000	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr17:57185000-57205600	Weak transcription	HSMMtube	muscle
41	chr17:57185000-57206800	Weak transcription	Pancreas	Pancrea
42	chr17:57185000-57211200	Weak transcription	Right Ventricle	heart
43	chr17:57185000-57212000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr17:57185000-57218800	Weak transcription	Fetal Intestine Large	intestine
45	chr17:57185000-57221600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr17:57185000-57231000	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr17:57185000-57231200	Weak transcription	Lung	lung
48	chr17:57185200-57186000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr17:57185200-57186000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr17:57185200-57186000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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