Variant report

Variant	nsv457576
Chromosome Location	chr16:81525637-81579433
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1572)
CpG islands
(count:1954)
Chromatin interactive
region (count:101)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1572 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:81528924-81528927	K562	blood:	n/a	n/a
2	ARID3A	chr16:81547245-81547583	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:81566312-81566544	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:81529158-81529984	K562	blood:	n/a	n/a
5	ARID3A	chr16:81567549-81568168	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:81538647-81538999	K562	blood:	n/a	n/a
7	ARID3A	chr16:81560007-81560151	K562	blood:	n/a	n/a
8	ARID3A	chr16:81544826-81545290	HepG2	liver:	n/a	n/a
9	ARID3A	chr16:81576143-81576703	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:81569226-81569512	HepG2	liver:	n/a	n/a
11	ATF1	chr16:81538547-81538994	K562	blood:	n/a	n/a
12	ATF1	chr16:81529312-81529767	K562	blood:	n/a	n/a
13	ATF1	chr16:81527276-81527612	K562	blood:	n/a	n/a
14	ATF1	chr16:81555575-81555990	K562	blood:	n/a	n/a
15	ATF1	chr16:81532692-81532837	K562	blood:	n/a	n/a
16	ATF2	chr16:81547449-81548101	GM12878	blood:	n/a	n/a
17	ATF2	chr16:81555591-81556030	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr16:81538531-81539353	GM12878	blood:	n/a	n/a
19	ATF3	chr16:81544695-81545268	A549	lung:	n/a	n/a
20	ATF3	chr16:81529187-81529838	K562	blood:	n/a	n/a
21	ATF3	chr16:81544835-81545326	A549	lung:	n/a	n/a
22	ATF3	chr16:81527245-81527602	K562	blood:	n/a	n/a
23	ATF3	chr16:81527280-81527553	K562	blood:	n/a	n/a
24	BACH1	chr16:81546872-81546994	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr16:81536075-81536121	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr16:81578312-81578549	GM12878	blood:	n/a	n/a
27	BCL3	chr16:81544754-81545337	A549	lung:	n/a	n/a
28	BCL3	chr16:81547091-81547702	A549	lung:	n/a	n/a
29	BCL3	chr16:81527056-81527888	A549	lung:	n/a	n/a
30	BCL3	chr16:81566178-81566816	A549	lung:	n/a	chr16:81566220-81566233
31	BCL3	chr16:81547189-81547745	A549	lung:	n/a	n/a
32	BCLAF1	chr16:81538797-81539387	GM12878	blood:	n/a	chr16:81539059-81539072 chr16:81539151-81539160
33	BCLAF1	chr16:81529199-81529961	K562	blood:	n/a	n/a
34	BCLAF1	chr16:81547276-81547924	GM12878	blood:	n/a	n/a
35	BHLHE40	chr16:81538606-81539165	K562	blood:	n/a	n/a
36	BHLHE40	chr16:81528733-81529808	K562	blood:	n/a	n/a
37	BHLHE40	chr16:81547567-81548087	GM12878	blood:	n/a	n/a
38	BHLHE40	chr16:81527141-81528110	K562	blood:	n/a	chr16:81527420-81527436
39	BHLHE40	chr16:81558183-81558240	K562	blood:	n/a	n/a
40	BHLHE40	chr16:81527378-81527578	A549	lung:	n/a	chr16:81527420-81527436
41	BHLHE40	chr16:81527288-81527606	HepG2	liver:	n/a	chr16:81527420-81527436
42	BHLHE40	chr16:81531532-81531643	GM12878	blood:	n/a	n/a
43	BHLHE40	chr16:81545055-81545240	HepG2	liver:	n/a	n/a
44	BHLHE40	chr16:81560650-81561016	K562	blood:	n/a	n/a
45	BHLHE40	chr16:81553458-81553784	GM12878	blood:	n/a	n/a
46	BRCA1	chr16:81577151-81577246	HepG2	liver:	n/a	n/a
47	BRCA1	chr16:81532819-81532846	HepG2	liver:	n/a	n/a
48	BRCA1	chr16:81527278-81527678	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr16:81547706-81548199	K562	blood:	n/a	n/a
50	CBX3	chr16:81528606-81529967	K562	blood:	n/a	n/a

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:81527427-81527477	T-47D	breast:	n/a
2	chr16:81565917-81565967	GM06990	blood:	n/a
3	chr16:81527427-81527477	T-47D	breast:	n/a
4	chr16:81565917-81565967	GM06990	blood:	n/a
5	chr16:81526361-81526411	HUVEC	blood vessel:	n/a
6	chr16:81533152-81533202	BE2_C	brain:	n/a
7	chr16:81529963-81530013	HRE	kidney:	n/a
8	chr16:81529963-81530013	IMR90	lung:	fetal
9	chr16:81547138-81547188	AG04450	lung:	fetal
10	chr16:81564527-81564577	PrEC	prostate:	n/a
11	chr16:81564553-81564603	Hela-S3	cervix:	n/a
12	chr16:81564192-81564242	T-47D	breast:	n/a
13	chr16:81529963-81530013	BJ	skin:	n/a
14	chr16:81529947-81529997	HRE	kidney:	n/a
15	chr16:81567375-81567425	NHDF-neo	bronchial:	n/a
16	chr16:81547907-81547957	IMR90	lung:	fetal
17	chr16:81577049-81577099	Jurkat	blood:	n/a
18	chr16:81526954-81527004	IMR90	lung:	fetal
19	chr16:81526361-81526411	GM19239	blood:	n/a
20	chr16:81527427-81527477	NHDF-neo	bronchial:	n/a
21	chr16:81526954-81527004	CMK	blood:	n/a
22	chr16:81527360-81527410	MCF-7	breast:	n/a
23	chr16:81526954-81527004	MCF-7	breast:	n/a
24	chr16:81564314-81564364	K562	blood:	n/a
25	chr16:81527360-81527410	Hela-S3	cervix:	n/a
26	chr16:81526361-81526411	GM12878	blood:	n/a
27	chr16:81572405-81572455	HL-60	blood:	n/a
28	chr16:81577049-81577099	A549	lung:	n/a
29	chr16:81527504-81527554	U87	brain:	n/a
30	chr16:81533152-81533202	U87	brain:	n/a
31	chr16:81564314-81564364	Hepatocyte	liver:	n/a
32	chr16:81547907-81547957	A549	lung:	n/a
33	chr16:81564192-81564242	NHDF-neo	bronchial:	n/a
34	chr16:81526361-81526411	PFSK-1	brain:	n/a
35	chr16:81527501-81527551	SK-N-SH	brain:	n/a
36	chr16:81577049-81577099	HRPEpiC	eye:	n/a
37	chr16:81572405-81572455	PANC-1	pancreas:	n/a
38	chr16:81579400-81579450	Hela-S3	cervix:	n/a
39	chr16:81528945-81528995	HEK293	kidney:	embryo
40	chr16:81526954-81527004	SK-N-SH_RA	brain:	n/a
41	chr16:81527504-81527554	AoSMC	blood vessel:	n/a
42	chr16:81527237-81527287	PFSK-1	brain:	n/a
43	chr16:81572405-81572455	ECC-1	luminal epithelium:	n/a
44	chr16:81565706-81565756	PANC-1	pancreas:	n/a
45	chr16:81527237-81527287	HCF	heart:	n/a
46	chr16:81567375-81567425	HCM	heart:	n/a
47	chr16:81528229-81528279	NHBE	bronchial:	n/a
48	chr16:81572405-81572455	GM12878	blood:	n/a
49	chr16:81564161-81564211	HIPEpiC	eye:	n/a
50	chr16:81564192-81564242	SK-N-SH_RA	brain:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr16:81534568..81536301-chr16:81536837..81539255,2	K562	blood:
2	chr16:81553683..81555515-chr16:81559365..81561780,2	MCF-7	breast:
3	chr16:81548752..81553118-chr16:81553470..81556973,6	K562	blood:
4	chr16:81436854..81437821-chr16:81571462..81572130,2	MCF-7	breast:
5	chr16:81575449..81577780-chr16:81580287..81583193,2	K562	blood:
6	chr16:81537410..81540431-chr16:81541653..81543691,3	K562	blood:
7	chr16:81527564..81530254-chr16:81556060..81557683,2	K562	blood:
8	chr16:81506233..81509171-chr16:81529935..81531469,2	MCF-7	breast:
9	chr16:81515452..81518298-chr16:81547120..81549781,2	MCF-7	breast:
10	chr16:81477859..81481266-chr16:81523834..81526339,3	MCF-7	breast:
11	chr16:81563450..81565897-chr16:81690369..81692226,2	K562	blood:
12	chr16:81576839..81579779-chr16:81583456..81585257,2	K562	blood:
13	chr16:81556103..81559286-chr16:81561998..81564976,3	K562	blood:
14	chr16:81534254..81537068-chr16:81537419..81539023,2	MCF-7	breast:
15	chr16:81535925..81538349-chr16:81544676..81546698,2	MCF-7	breast:
16	chr16:81537410..81540431-chr16:81541653..81543691,3	K562	blood:
17	chr16:81578943..81580979-chr16:81604433..81607387,2	K562	blood:
18	chr16:81486409..81487978-chr16:81548913..81551529,2	K562	blood:
19	chr16:81481928..81485099-chr16:81576354..81580756,4	K562	blood:
20	chr16:81560475..81564171-chr16:81564775..81571060,7	K562	blood:
21	chr16:81534254..81537068-chr16:81537419..81539023,2	MCF-7	breast:
22	chr16:81550713..81552453-chr16:81584328..81586999,2	K562	blood:
23	chr16:81478269..81480655-chr16:81559515..81562675,4	MCF-7	breast:
24	chr16:81545018..81547272-chr16:81553455..81555320,2	MCF-7	breast:
25	chr16:81540223..81542527-chr16:81557880..81560603,2	K562	blood:
26	chr16:81476822..81479616-chr16:81528551..81531319,2	MCF-7	breast:
27	chr16:81538598..81540305-chr16:81552129..81554762,2	K562	blood:
28	chr16:81575502..81578399-chr16:81587269..81589357,4	MCF-7	breast:
29	chr16:81478553..81481266-chr16:81577586..81580261,2	MCF-7	breast:
30	chr16:81480285..81482687-chr16:81557234..81559498,2	K562	blood:
31	chr16:81568196..81570082-chr16:81573508..81576113,2	K562	blood:
32	chr1:11967644..11970692-chr16:81526745..81530304,3	K562	blood:
33	chr16:81547505..81549676-chr16:81576353..81579232,2	MCF-7	breast:
34	chr16:81534568..81536301-chr16:81536837..81539255,2	K562	blood:
35	chr16:81490986..81492646-chr16:81531978..81534213,2	MCF-7	breast:
36	chr16:81541404..81543131-chr16:81562418..81564438,2	MCF-7	breast:
37	chr16:81477821..81480197-chr16:81532680..81534893,2	MCF-7	breast:
38	chr16:81478427..81480375-chr16:81529465..81532019,2	MCF-7	breast:
39	chr16:81557086..81559213-chr16:81591248..81592791,2	MCF-7	breast:
40	chr16:81571814..81573956-chr16:81577277..81579755,3	K562	blood:
41	chr16:81520528..81523163-chr16:81525818..81527534,2	MCF-7	breast:
42	chr16:81569545..81572844-chr16:81574996..81578300,3	MCF-7	breast:
43	chr16:81547505..81549676-chr16:81576353..81579232,2	MCF-7	breast:
44	chr16:81571814..81573956-chr16:81577277..81579755,3	K562	blood:
45	chr16:81477278..81479557-chr16:81555810..81558008,2	MCF-7	breast:
46	chr16:81538598..81540305-chr16:81552129..81554762,2	K562	blood:
47	chr16:81556103..81558627-chr16:81562997..81564545,2	K562	blood:
48	chr16:81565757..81568380-chr16:81569280..81572909,4	K562	blood:
49	chr16:81549027..81553526-chr16:81553827..81556992,4	MCF-7	breast:
50	chr16:81541404..81543131-chr16:81562418..81564438,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7854-3p	chr16:81567547-81567567	MIMAT0030429

No data

Variant related genes	Relation type
CMIP	TF binding region
CMIP	CpG island
ENSG00000153815	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000201801	chromatin interactions

Extended variants
information (count: 2767 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2767 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12445748	chr16:81525637-81525638	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527938337	chr16:81525663-81525664	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs542929574	chr16:81525667-81525668	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs374690121	chr16:81525669-81525670	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs561296206	chr16:81525684-81525685	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531960345	chr16:81525687-81525688	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs558090970	chr16:81525691-81525692	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs549596207	chr16:81525698-81525699	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs117802027	chr16:81525713-81525714	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs571724986	chr16:81525726-81525727	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs2926004	chr16:81525727-81525728	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs547372383	chr16:81525769-81525770	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs565691585	chr16:81525781-81525782	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs536519283	chr16:81525789-81525790	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs184639072	chr16:81525804-81525805	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs569733545	chr16:81525840-81525841	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs554073535	chr16:81525879-81525880	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs537289477	chr16:81525886-81525887	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs556376887	chr16:81525918-81525919	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs76081613	chr16:81525919-81525920	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs545107548	chr16:81525956-81525957	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs187617336	chr16:81525990-81525991	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs142697768	chr16:81526021-81526022	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs542930688	chr16:81526023-81526024	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs572613783	chr16:81526039-81526040	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs75337513	chr16:81526045-81526046	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs531802980	chr16:81526069-81526070	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs373075260	chr16:81526070-81526071	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs115924163	chr16:81526100-81526101	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs562997059	chr16:81526121-81526122	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376862596	chr16:81526137-81526138	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs143846888	chr16:81526170-81526171	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs547533129	chr16:81526172-81526173	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs56682366	chr16:81526180-81526181	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs202103560	chr16:81526188-81526189	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs35195572	chr16:81526222-81526223	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs565654901	chr16:81526247-81526248	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529747283	chr16:81526262-81526263	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs558658798	chr16:81526270-81526271	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs115004261	chr16:81526288-81526289	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs113030351	chr16:81526295-81526296	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs7193307	chr16:81526302-81526303	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs148576084	chr16:81526349-81526350	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs375547243	chr16:81526350-81526351	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs117332614	chr16:81526361-81526362	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs545491308	chr16:81526407-81526408	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs538719013	chr16:81526419-81526420	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs142978132	chr16:81526426-81526427	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs374010296	chr16:81526436-81526437	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs572092228	chr16:81526461-81526462	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2787 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81506000-81546600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr16:81506600-81547000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr16:81510400-81533200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr16:81511400-81527000	Enhancers	Fetal Muscle Leg	muscle
5	chr16:81515200-81531600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr16:81515200-81532600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr16:81516400-81525800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr16:81516400-81525800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr16:81516600-81525800	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr16:81517400-81526400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr16:81517400-81526600	Weak transcription	Hela-S3	cervix
12	chr16:81517400-81531600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr16:81517600-81526800	Genic enhancers	A549	lung
14	chr16:81518200-81527000	Weak transcription	Thymus	Thymus
15	chr16:81519600-81532000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr16:81519800-81527200	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr16:81520200-81525800	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr16:81520400-81532200	Enhancers	Spleen	Spleen
19	chr16:81520600-81526800	Weak transcription	Dnd41	blood
20	chr16:81520800-81527400	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr16:81521000-81528600	Weak transcription	Primary T cells from cord blood	blood
22	chr16:81521200-81525800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr16:81521200-81526000	Weak transcription	Stomach Smooth Muscle	stomach
24	chr16:81522000-81526400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr16:81522200-81528800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr16:81522400-81526600	Weak transcription	NHEK	skin
27	chr16:81522400-81528400	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr16:81522400-81537000	Enhancers	HUVEC	blood vessel
29	chr16:81522600-81528400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr16:81522600-81528800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr16:81522600-81529800	Enhancers	Esophagus	oesophagus
32	chr16:81522600-81532200	Enhancers	Fetal Muscle Trunk	muscle
33	chr16:81522800-81525800	Weak transcription	Fetal Intestine Large	intestine
34	chr16:81522800-81529800	Enhancers	Placenta	Placenta
35	chr16:81523200-81526800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr16:81523400-81525800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr16:81523400-81526000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr16:81523400-81526800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr16:81523600-81525800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr16:81523600-81525800	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr16:81523600-81527600	Enhancers	Fetal Brain Male	brain
42	chr16:81523600-81531800	Enhancers	Stomach Mucosa	stomach
43	chr16:81523800-81525800	Weak transcription	Fetal Thymus	thymus
44	chr16:81523800-81528200	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr16:81523800-81529000	Weak transcription	Ovary	ovary
46	chr16:81523800-81530800	Weak transcription	Colon Smooth Muscle	Colon
47	chr16:81524000-81526200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr16:81524000-81526800	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr16:81524000-81531000	Weak transcription	GM12878-XiMat	blood
50	chr16:81524200-81529800	Enhancers	Gastric	stomach

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