Variant report

Variant	esv1824966
Chromosome Location	chr4:78747771-78823070
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1212)
CpG islands
(count:671)
Chromatin interactive
region (count:89)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1212 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:78803040-78803425	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:78794149-78794584	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:78783005-78784318	K562	blood:	n/a	n/a
4	ARID3A	chr4:78782650-78784400	HepG2	liver:	n/a	n/a
5	ATF1	chr4:78783658-78784371	K562	blood:	n/a	n/a
6	ATF2	chr4:78783685-78784256	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:78783647-78784269	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:78782897-78784470	GM12878	blood:	n/a	n/a
9	ATF2	chr4:78782632-78784606	GM12878	blood:	n/a	n/a
10	ATF3	chr4:78783601-78784128	A549	lung:	n/a	chr4:78783875-78783884
11	ATF3	chr4:78783558-78784156	A549	lung:	n/a	chr4:78783875-78783884
12	ATF3	chr4:78783671-78784134	K562	blood:	n/a	chr4:78783875-78783884
13	BACH1	chr4:78783621-78784483	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:78803056-78803367	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr4:78782693-78783011	GM12878	blood:	n/a	chr4:78782859-78782870
16	BATF	chr4:78783132-78783331	GM12878	blood:	n/a	n/a
17	BATF	chr4:78783661-78784095	GM12878	blood:	n/a	n/a
18	BATF	chr4:78782701-78782974	GM12878	blood:	n/a	chr4:78782859-78782870
19	BATF	chr4:78783069-78783390	GM12878	blood:	n/a	n/a
20	BCL3	chr4:78783460-78784271	A549	lung:	n/a	n/a
21	BCL3	chr4:78783555-78784248	A549	lung:	n/a	n/a
22	BCLAF1	chr4:78782875-78784454	GM12878	blood:	n/a	chr4:78784363-78784370
23	BCLAF1	chr4:78783521-78784288	K562	blood:	n/a	n/a
24	BCLAF1	chr4:78782946-78784375	GM12878	blood:	n/a	chr4:78784363-78784370
25	BCLAF1	chr4:78783486-78784316	K562	blood:	n/a	n/a
26	BHLHE40	chr4:78783699-78784201	HepG2	liver:	n/a	n/a
27	BHLHE40	chr4:78794383-78794524	HepG2	liver:	n/a	n/a
28	BHLHE40	chr4:78783030-78784383	K562	blood:	n/a	n/a
29	BHLHE40	chr4:78782821-78784614	GM12878	blood:	n/a	n/a
30	BRCA1	chr4:78783737-78784456	HepG2	liver:	n/a	n/a
31	BRCA1	chr4:78783178-78784109	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr4:78815281-78815339	GM12878	blood:	n/a	n/a
33	BRCA1	chr4:78783476-78784135	H1-hESC	embryonic stem cell:	n/a	n/a
34	CBX3	chr4:78783651-78784311	K562	blood:	n/a	n/a
35	CBX3	chr4:78783579-78784465	K562	blood:	n/a	n/a
36	CCNT2	chr4:78783060-78784466	K562	blood:	n/a	chr4:78784353-78784373
37	CEBPB	chr4:78784400-78784734	K562	blood:	n/a	n/a
38	CEBPB	chr4:78813228-78813471	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr4:78784420-78784781	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:78761664-78761864	K562	blood:	n/a	n/a
41	CEBPB	chr4:78803096-78803428	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:78783636-78784642	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr4:78803129-78803349	A549	lung:	n/a	n/a
44	CEBPB	chr4:78784421-78784694	K562	blood:	n/a	n/a
45	CEBPB	chr4:78813308-78813412	K562	blood:	n/a	n/a
46	CEBPB	chr4:78783560-78784236	A549	lung:	n/a	n/a
47	CEBPB	chr4:78812521-78812625	K562	blood:	n/a	n/a
48	CEBPB	chr4:78794010-78794223	HepG2	liver:	n/a	n/a
49	CEBPB	chr4:78794238-78794558	HepG2	liver:	n/a	chr4:78794366-78794377
50	CEBPB	chr4:78761645-78761830	HepG2	liver:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78784263-78784313	GM12892	blood:	n/a
2	chr4:78783977-78784027	HRCEpiC	kidney:	n/a
3	chr4:78783977-78784027	HEK293	kidney:	embryo
4	chr4:78783825-78783875	NH-A	brain:	n/a
5	chr4:78783082-78783132	HRPEpiC	eye:	n/a
6	chr4:78784263-78784313	NH-A	brain:	n/a
7	chr4:78782057-78782107	PFSK-1	brain:	n/a
8	chr4:78783825-78783875	SK-N-SH	brain:	n/a
9	chr4:78784105-78784155	PANC-1	pancreas:	n/a
10	chr4:78783082-78783132	SKMC	muscle:	n/a
11	chr4:78783082-78783132	PrEC	prostate:	n/a
12	chr4:78787669-78787719	Hela-S3	cervix:	n/a
13	chr4:78783082-78783132	HIPEpiC	eye:	n/a
14	chr4:78783082-78783132	HCM	heart:	n/a
15	chr4:78783082-78783132	NB4	blood:	n/a
16	chr4:78783977-78784027	HCF	heart:	n/a
17	chr4:78783082-78783132	SK-N-SH	brain:	n/a
18	chr4:78783538-78783588	AG09319	gingival:	n/a
19	chr4:78783977-78784027	SKMC	muscle:	n/a
20	chr4:78783825-78783875	IMR90	lung:	fetal
21	chr4:78783746-78783796	SKMC	muscle:	n/a
22	chr4:78784105-78784155	NHDF-neo	bronchial:	n/a
23	chr4:78783977-78784027	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:78783746-78783796	HEEpiC	esophagus:	n/a
25	chr4:78782057-78782107	NH-A	brain:	n/a
26	chr4:78783746-78783796	GM12878	blood:	n/a
27	chr4:78782057-78782107	GM19239	blood:	n/a
28	chr4:78783746-78783796	HL-60	blood:	n/a
29	chr4:78784105-78784155	Jurkat	blood:	n/a
30	chr4:78783799-78783849	AG09319	gingival:	n/a
31	chr4:78783977-78784027	SAEC	small airway:	n/a
32	chr4:78784105-78784155	K562	blood:	n/a
33	chr4:78782057-78782107	A549	lung:	n/a
34	chr4:78783082-78783132	BJ	skin:	n/a
35	chr4:78784263-78784313	HepG2	liver:	n/a
36	chr4:78783799-78783849	K562	blood:	n/a
37	chr4:78783799-78783849	Jurkat	blood:	n/a
38	chr4:78783538-78783588	NT2-D1	testis:	n/a
39	chr4:78783746-78783796	HUVEC	blood vessel:	n/a
40	chr4:78783082-78783132	HepG2	liver:	n/a
41	chr4:78783977-78784027	BJ	skin:	n/a
42	chr4:78783825-78783875	Hepatocyte	liver:	n/a
43	chr4:78787669-78787719	AG09319	gingival:	n/a
44	chr4:78784105-78784155	MCF-7	breast:	n/a
45	chr4:78783746-78783796	H1-hESC	embryonic stem cell:	embryo
46	chr4:78783825-78783875	LNCaP	prostate:	n/a
47	chr4:78784263-78784313	IMR90	lung:	fetal
48	chr4:78783825-78783875	SAEC	small airway:	n/a
49	chr4:78783746-78783796	SK-N-SH	brain:	n/a
50	chr4:78783799-78783849	H1-hESC	embryonic stem cell:	embryo

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:78740242..78743124-chr4:78774584..78777185,2	K562	blood:
2	chr4:78740250..78742627-chr4:78801461..78803868,2	MCF-7	breast:
3	chr4:78783655..78785573-chr4:78787222..78790080,4	MCF-7	breast:
4	chr4:78774745..78780224-chr4:78780952..78785621,18	K562	blood:
5	chr4:78762303..78763958-chr4:78782788..78784420,2	K562	blood:
6	chr4:78783060..78785157-chr4:78820001..78822393,2	MCF-7	breast:
7	chr4:78782853..78785738-chr4:78785814..78790538,6	MCF-7	breast:
8	chr4:78780319..78783201-chr4:78783886..78786015,3	K562	blood:
9	chr4:78752734..78755481-chr4:78760331..78761862,2	MCF-7	breast:
10	chr4:78751560..78754519-chr4:78789849..78792401,2	K562	blood:
11	chr4:78733342..78735297-chr4:78791961..78793861,2	K562	blood:
12	chr4:78783859..78785659-chr4:78829258..78831450,2	K562	blood:
13	chr4:78766322..78768187-chr4:78776511..78778748,2	K562	blood:
14	chr4:78783315..78786116-chr4:78803157..78806156,2	MCF-7	breast:
15	chr4:77872181..77874980-chr4:78778372..78781139,2	MCF-7	breast:
16	chr4:78740102..78741887-chr4:78811367..78813986,2	K562	blood:
17	chr4:78754144..78756097-chr4:78756156..78760285,3	MCF-7	breast:
18	chr4:78744788..78747735-chr4:78750075..78752485,4	K562	blood:
19	chr4:78783567..78785320-chr4:78814122..78816828,2	K562	blood:
20	chr4:78783315..78786116-chr4:78803157..78806156,2	MCF-7	breast:
21	chr4:78798979..78800578-chr4:78800751..78803601,2	K562	blood:
22	chr4:78782853..78785738-chr4:78785814..78790538,6	MCF-7	breast:
23	chr4:78754144..78756097-chr4:78756156..78760285,3	MCF-7	breast:
24	chr4:78778939..78781119-chr4:78782417..78784087,3	MCF-7	breast:
25	chr4:78782527..78785375-chr4:78792236..78798548,6	MCF-7	breast:
26	chr4:78752734..78755481-chr4:78760331..78761862,2	MCF-7	breast:
27	chr19:39900040..39900831-chr4:78783308..78783809,2	Hela-S3	cervix:
28	chr4:78738995..78744410-chr4:78782336..78785612,12	K562	blood:
29	chr4:78746598..78749017-chr4:78782763..78785297,2	MCF-7	breast:
30	chr4:78817939..78819468-chr4:78825974..78827657,2	MCF-7	breast:
31	chr4:78801600..78804002-chr4:78805552..78808454,2	K562	blood:
32	chr4:78740459..78743070-chr4:78773360..78775047,2	MCF-7	breast:
33	chr4:78739885..78741422-chr4:78754465..78756527,2	K562	blood:
34	chr12:51157111..51157871-chr4:78784453..78785369,2	Hela-S3	cervix:
35	chr4:78759168..78761864-chr4:78783696..78785578,2	K562	blood:
36	chr4:78750079..78752870-chr4:78754629..78757653,3	K562	blood:
37	chr4:78815836..78817372-chr4:78817418..78819498,2	K562	blood:
38	chr4:78811376..78813925-chr4:78816983..78819701,2	K562	blood:
39	chr4:78740068..78741802-chr4:78757665..78759497,2	K562	blood:
40	chr4:78738764..78744926-chr4:78780904..78785516,9	MCF-7	breast:
41	chr4:78786547..78788323-chr4:78797006..78799042,2	K562	blood:
42	chr4:78788439..78790462-chr4:78797402..78799471,2	K562	blood:
43	chr4:78785570..78789084-chr4:78790216..78793354,5	K562	blood:
44	chr4:78819042..78822002-chr4:78825525..78828218,2	K562	blood:
45	chr4:78738972..78741487-chr4:78821342..78824641,3	K562	blood:
46	chr4:78734703..78743448-chr4:78779372..78785561,20	K562	blood:
47	chr4:78774429..78778317-chr4:78782409..78784960,4	MCF-7	breast:
48	chr4:78739526..78741984-chr4:78787017..78789736,2	MCF-7	breast:
49	chr4:78782878..78784636-chr4:78792721..78794473,2	MCF-7	breast:
50	chr4:78791921..78794709-chr4:78802036..78804705,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRAS1-1	chr4:78792898-78793009	NONHSAT097059
2	lnc-FRAS1-1	chr4:78784022-78784167	NONHSAT097059
3	lnc-FRAS1-1	chr4:78806410-78806472	NONHSAT097059
4	lnc-FRAS1-1	chr4:78804396-78804654	NONHSAT097059
5	lnc-CNOT6L-2	chr4:78785662-78785958	NONHSAT097060

No data

Variant related genes	Relation type
ENSG00000250214	TF binding region
MRPL1	TF binding region
ENSG00000250214	CpG island
MRPL1	CpG island
ENSG00000266559	chromatin interactions
ENSG00000138767	chromatin interactions
ENSG00000123268	chromatin interactions
ENSG00000169288	chromatin interactions
ENSG00000250214	chromatin interactions

Extended variants
information (count: 2539 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2539 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4365752	chr4:78747771-78747772	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186962055	chr4:78747824-78747825	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558711151	chr4:78747844-78747845	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs543276455	chr4:78747922-78747923	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs191617879	chr4:78747950-78747951	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529174673	chr4:78747965-78747966	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575220956	chr4:78747977-78747978	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548911480	chr4:78748015-78748016	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544344066	chr4:78748025-78748026	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs116567943	chr4:78748027-78748028	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs141057019	chr4:78748032-78748033	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs551039259	chr4:78748036-78748037	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs201963583	chr4:78748056-78748057	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs150107762	chr4:78748065-78748066	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs537616617	chr4:78748114-78748115	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs184914055	chr4:78748155-78748156	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs540558838	chr4:78748191-78748192	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs567902013	chr4:78748202-78748203	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs188231628	chr4:78748212-78748213	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs553745941	chr4:78748214-78748215	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573261221	chr4:78748260-78748261	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545449910	chr4:78748276-78748277	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs540388556	chr4:78748283-78748284	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs34299608	chr4:78748332-78748333	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs551168528	chr4:78748431-78748432	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs193178284	chr4:78748522-78748523	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs115989424	chr4:78748549-78748550	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs371363940	chr4:78748631-78748632	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs75018080	chr4:78748638-78748639	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566160012	chr4:78748648-78748649	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs370313575	chr4:78748650-78748651	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs529092358	chr4:78748686-78748687	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs35210418	chr4:78748709-78748710	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs17002816	chr4:78748751-78748752	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs559249249	chr4:78748768-78748769	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs77149973	chr4:78748776-78748777	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550977993	chr4:78748826-78748827	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs367612262	chr4:78748838-78748839	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs185289924	chr4:78748859-78748860	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs550698636	chr4:78748925-78748926	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs72868204	chr4:78748926-78748927	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs536883922	chr4:78748950-78748951	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs553682874	chr4:78748969-78748970	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1996740	chr4:78748977-78748978	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs2866688	chr4:78749042-78749043	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs558680850	chr4:78749091-78749092	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372022016	chr4:78749127-78749128	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs189273409	chr4:78749172-78749173	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs111322562	chr4:78749183-78749184	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548306149	chr4:78749192-78749193	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1836 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78743200-78750000	Enhancers	Primary T cells fromperipheralblood	blood
2	chr4:78743400-78749800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
3	chr4:78743400-78750200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr4:78743800-78747800	Weak transcription	Dnd41	blood
5	chr4:78743800-78748200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr4:78744000-78748600	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr4:78744200-78748200	Weak transcription	Primary hematopoietic stem cells	blood
8	chr4:78744400-78748600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr4:78744600-78748400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr4:78745000-78747800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr4:78746600-78749800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr4:78746800-78750000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr4:78746800-78750000	Enhancers	Thymus	Thymus
14	chr4:78747000-78747800	Enhancers	Primary B cells from cord blood	blood
15	chr4:78747000-78749600	Enhancers	Primary B cells from peripheral blood	blood
16	chr4:78747000-78750000	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr4:78747000-78750400	Enhancers	Primary T cells from cord blood	blood
18	chr4:78747000-78750600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr4:78747000-78750800	Enhancers	Fetal Thymus	thymus
20	chr4:78747200-78748600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr4:78747200-78749000	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr4:78747200-78750600	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr4:78747400-78748200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr4:78747400-78748600	Enhancers	GM12878-XiMat	blood
25	chr4:78747600-78748000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr4:78747800-78748800	Flanking Active TSS	Primary B cells from cord blood	blood
27	chr4:78747800-78749800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr4:78747800-78750600	Enhancers	Dnd41	blood
29	chr4:78748000-78749600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr4:78748200-78748400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
31	chr4:78748200-78748400	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr4:78748200-78748600	Enhancers	Primary hematopoietic stem cells	blood
33	chr4:78748400-78748800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr4:78748400-78749000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr4:78748600-78748800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
36	chr4:78748600-78748800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr4:78748600-78749000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:78748800-78749000	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr4:78748800-78749000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr4:78748800-78749200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
41	chr4:78748800-78749600	Enhancers	Primary B cells from cord blood	blood
42	chr4:78749000-78749200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
43	chr4:78749000-78749200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr4:78749000-78749400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
45	chr4:78749200-78749800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr4:78749200-78750000	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr4:78749400-78750000	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr4:78750400-78750600	Enhancers	K562	blood
49	chr4:78753400-78754600	Enhancers	NHEK	skin
50	chr4:78753600-78755000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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