Variant report

Variant	esv3373756
Chromosome Location	chr6:15661798-15664346
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:453)
CpG islands
(count:978)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:15662901-15662999	HepG2	liver:	n/a	n/a
2	ATF2	chr6:15662399-15662941	GM12878	blood:	n/a	n/a
3	ATF3	chr6:15662955-15663393	K562	blood:	n/a	n/a
4	ATF3	chr6:15662588-15662866	K562	blood:	n/a	chr6:15662824-15662838
5	ATF3	chr6:15662486-15662859	HepG2	liver:	n/a	chr6:15662824-15662838
6	BACH1	chr6:15663025-15663406	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr6:15662327-15662890	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:15662413-15663500	GM12878	blood:	n/a	chr6:15663130-15663146 chr6:15663138-15663154 chr6:15663103-15663119
9	BHLHE40	chr6:15662456-15663327	HepG2	liver:	n/a	chr6:15663130-15663146 chr6:15663138-15663154 chr6:15663103-15663119
10	BHLHE40	chr6:15662446-15663369	K562	blood:	n/a	chr6:15663130-15663146 chr6:15663138-15663154 chr6:15663103-15663119
11	BRCA1	chr6:15663124-15663129	HepG2	liver:	n/a	n/a
12	CBX3	chr6:15662378-15663928	K562	blood:	n/a	n/a
13	CCNT2	chr6:15662385-15663439	K562	blood:	n/a	n/a
14	CEBPD	chr6:15662726-15663365	HepG2	liver:	n/a	n/a
15	CHD1	chr6:15662424-15662884	GM12878	blood:	n/a	n/a
16	CHD2	chr6:15663177-15663296	HepG2	liver:	n/a	n/a
17	CHD2	chr6:15662428-15663389	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr6:15662437-15663443	GM12878	blood:	n/a	n/a
19	CHD2	chr6:15662512-15662833	K562	blood:	n/a	n/a
20	CHD2	chr6:15662728-15662767	HepG2	liver:	n/a	n/a
21	CREB1	chr6:15662313-15663546	HepG2	liver:	n/a	n/a
22	CTBP2	chr6:15662313-15663235	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr6:15663040-15663190	HEK293	kidney:	n/a	chr6:15663154-15663164
24	CTCF	chr6:15663096-15663209	MCF-7	breast:	n/a	chr6:15663154-15663164
25	CTCF	chr6:15662679-15662684	MCF-7	breast:	n/a	n/a
26	CTCF	chr6:15662540-15662690	GM12871	blood:	n/a	n/a
27	CTCF	chr6:15663040-15663190	GM12872	blood:	n/a	chr6:15663154-15663164
28	CTCF	chr6:15663000-15663150	HRE	kidney:	n/a	n/a
29	CTCF	chr6:15662460-15662610	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr6:15663040-15663190	GM12868	blood:	n/a	chr6:15663154-15663164
31	CTCF	chr6:15662603-15662659	MCF-7	breast:	n/a	n/a
32	CTCF	chr6:15662860-15663010	BJ	skin:	n/a	n/a
33	CTCF	chr6:15662584-15662645	Fibrobl	skin:	n/a	n/a
34	CTCF	chr6:15663040-15663190	SK-N-SH_RA	brain:	n/a	chr6:15663154-15663164
35	CTCF	chr6:15663100-15663250	GM12869	blood:	n/a	chr6:15663154-15663164
36	CTCF	chr6:15663060-15663210	K562	blood:	n/a	chr6:15663154-15663164
37	CTCF	chr6:15662500-15662650	GM12871	blood:	n/a	n/a
38	CTCF	chr6:15663142-15663355	Spleen_OC	spleen:	n/a	chr6:15663154-15663164
39	CTCF	chr6:15663060-15663210	GM12878	blood:	n/a	chr6:15663154-15663164
40	CTCF	chr6:15662674-15662675	GM19240	blood:	n/a	n/a
41	CTCF	chr6:15663040-15663190	WERI-Rb-1	eye:	n/a	chr6:15663154-15663164
42	CTCF	chr6:15663113-15663196	H1-hESC	embryonic stem cell:	n/a	chr6:15663154-15663164
43	CTCF	chr6:15662500-15662650	GM12878	blood:	n/a	n/a
44	CTCF	chr6:15663107-15663228	GM12891	blood:	n/a	chr6:15663154-15663164
45	CTCF	chr6:15663080-15663230	Caco-2	colon:	n/a	chr6:15663154-15663164
46	CTCF	chr6:15662500-15662650	GM12872	blood:	n/a	n/a
47	CTCF	chr6:15662820-15662970	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr6:15663081-15663213	MCF-7	breast:	n/a	chr6:15663154-15663164
49	CTCF	chr6:15662565-15662678	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:15662595-15662715	GM12891	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:15662223-15662273	HRPEpiC	eye:	n/a
2	chr6:15663468-15663518	HCF	heart:	n/a
3	chr6:15662223-15662273	HRPEpiC	eye:	n/a
4	chr6:15663468-15663518	HCF	heart:	n/a
5	chr6:15662764-15662814	LNCaP	prostate:	n/a
6	chr6:15663468-15663518	GM06990	blood:	n/a
7	chr6:15663356-15663406	Caco-2	colon:	n/a
8	chr6:15663448-15663498	HAEpiC	amniotic membrane:	n/a
9	chr6:15662764-15662814	HCM	heart:	n/a
10	chr6:15663134-15663184	IMR90	lung:	fetal
11	chr6:15663344-15663394	ovcar-3	ovarian:	n/a
12	chr6:15662448-15662498	HRE	kidney:	n/a
13	chr6:15662223-15662273	Hepatocyte	liver:	n/a
14	chr6:15663024-15663074	SK-N-MC	brain:	n/a
15	chr6:15663501-15663551	K562	blood:	n/a
16	chr6:15662707-15662757	HUVEC	blood vessel:	n/a
17	chr6:15663356-15663406	HepG2	liver:	n/a
18	chr6:15662223-15662273	U87	brain:	n/a
19	chr6:15663468-15663518	NT2-D1	testis:	n/a
20	chr6:15663501-15663551	HL-60	blood:	n/a
21	chr6:15663344-15663394	HRE	kidney:	n/a
22	chr6:15662448-15662498	RPTEC	kidney:	n/a
23	chr6:15663448-15663498	HCPEpiC	choroid plexus:	n/a
24	chr6:15663356-15663406	HCF	heart:	n/a
25	chr6:15663356-15663406	IMR90	lung:	fetal
26	chr6:15663356-15663406	HPAEpiC	pulmonary alveolar:	n/a
27	chr6:15663501-15663551	Jurkat	blood:	n/a
28	chr6:15663360-15663410	HCM	heart:	n/a
29	chr6:15663538-15663588	ovcar-3	ovarian:	n/a
30	chr6:15662223-15662273	HMEC	breast:	n/a
31	chr6:15663170-15663220	SK-N-SH	brain:	n/a
32	chr6:15663442-15663492	PFSK-1	brain:	n/a
33	chr6:15663024-15663074	AG04449	skin:	fetal
34	chr6:15662764-15662814	ProgFib	skin:	n/a
35	chr6:15663448-15663498	SK-N-SH	brain:	n/a
36	chr6:15662764-15662814	NT2-D1	testis:	n/a
37	chr6:15663448-15663498	AoSMC	blood vessel:	n/a
38	chr6:15662764-15662814	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:15663356-15663406	HL-60	blood:	n/a
40	chr6:15663501-15663551	Caco-2	colon:	n/a
41	chr6:15663538-15663588	MCF-7	breast:	n/a
42	chr6:15662223-15662273	HEEpiC	esophagus:	n/a
43	chr6:15662448-15662498	U87	brain:	n/a
44	chr6:15663170-15663220	AG04450	lung:	fetal
45	chr6:15664231-15664281	SAEC	small airway:	n/a
46	chr6:15663468-15663518	NHDF-neo	bronchial:	n/a
47	chr6:15662707-15662757	SAEC	small airway:	n/a
48	chr6:15663344-15663394	MCF10A-Er-Src	breast:	n/a
49	chr6:15663170-15663220	NB4	blood:	n/a
50	chr6:15663170-15663220	HPAEpiC	pulmonary alveolar:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:15655170..15659272-chr6:15659508..15662983,5	MCF-7	breast:
2	chr1:153621962..153623668-chr6:15660534..15662735,2	MCF-7	breast:
3	chr6:15660394..15662870-chr6:15679792..15681475,2	K562	blood:
4	chr6:15570441..15572799-chr6:15659666..15662053,2	K562	blood:
5	chr6:15659552..15664792-chr6:16126837..16130644,6	MCF-7	breast:
6	chr6:15661311..15664347-chr6:16127901..16131243,6	K562	blood:
7	chr6:15661088..15663422-chr6:16128985..16131574,3	K562	blood:

No data

Variant related genes	Relation type
DTNBP1	TF binding region
DTNBP1	CpG island
ENSG00000007944	chromatin interactions

Extended variants
information (count: 93 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545108667	chr6:15661811-15661812	Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141739976	chr6:15661843-15661844	Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs200190961	chr6:15661876-15661877	Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs150839590	chr6:15661892-15661893	Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs541292865	chr6:15661913-15661914	Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs28502274	chr6:15662012-15662013	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs561155639	chr6:15662013-15662014	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530185611	chr6:15662046-15662047	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs554429236	chr6:15662058-15662059	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs549958310	chr6:15662061-15662062	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs569689985	chr6:15662261-15662262	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs139319306	chr6:15662321-15662322	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs114874683	chr6:15662322-15662323	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs144185767	chr6:15662393-15662394	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs534929952	chr6:15662442-15662443	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs370628932	chr6:15662488-15662489	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs568363311	chr6:15662494-15662495	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs537286617	chr6:15662497-15662498	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368836615	chr6:15662502-15662503	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs557105153	chr6:15662551-15662552	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs576490670	chr6:15662573-15662574	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545457381	chr6:15662575-15662576	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558696903	chr6:15662580-15662581	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572069825	chr6:15662581-15662582	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541329347	chr6:15662582-15662583	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs186424981	chr6:15662589-15662590	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs574781125	chr6:15662611-15662612	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543688058	chr6:15662614-15662615	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372921303	chr6:15662672-15662673	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs563881992	chr6:15662690-15662691	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs190906727	chr6:15662766-15662767	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs372652603	chr6:15662778-15662779	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs146173212	chr6:15662780-15662781	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559397217	chr6:15662782-15662783	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs59686948	chr6:15662783-15662784	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs548201290	chr6:15662784-15662785	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs71535046	chr6:15662785-15662786	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs9476887	chr6:15662891-15662892	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs537322213	chr6:15662893-15662894	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs577520812	chr6:15662912-15662913	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs550524922	chr6:15662964-15662965	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs570591940	chr6:15662966-15662967	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs538766228	chr6:15663002-15663003	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs370226322	chr6:15663006-15663007	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs373449292	chr6:15663016-15663017	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201375623	chr6:15663017-15663018	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs201270780	chr6:15663028-15663029	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs376357111	chr6:15663035-15663036	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs368994656	chr6:15663045-15663046	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs150529889	chr6:15663089-15663090	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
abnormal development	18461090	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17142309	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian cancer	20844748	CNVD
Developmental delay	19490664	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Schizophrenia	22423091	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:546 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15615200-15662200	Weak transcription	Gastric	stomach
2	chr6:15616800-15662000	Weak transcription	Placenta	Placenta
3	chr6:15616800-15662200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:15621800-15662200	Weak transcription	Pancreas	Pancrea
5	chr6:15623800-15662000	Weak transcription	Stomach Smooth Muscle	stomach
6	chr6:15628600-15662000	Weak transcription	NHLF	lung
7	chr6:15629600-15661800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr6:15632200-15662000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr6:15637200-15662000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr6:15638200-15662000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr6:15639400-15662200	Weak transcription	Left Ventricle	heart
12	chr6:15642000-15662000	Weak transcription	Brain Angular Gyrus	brain
13	chr6:15642200-15662200	Weak transcription	Aorta	Aorta
14	chr6:15642600-15662200	Weak transcription	Esophagus	oesophagus
15	chr6:15642800-15662000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:15642800-15662000	Weak transcription	Lung	lung
17	chr6:15642800-15662000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr6:15643000-15662000	Weak transcription	Fetal Stomach	stomach
19	chr6:15644400-15661800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr6:15644400-15662000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:15644800-15661800	Weak transcription	HepG2	liver
22	chr6:15644800-15662000	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr6:15644800-15662000	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr6:15645600-15661800	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr6:15646000-15662000	Weak transcription	NHDF-Ad	bronchial
26	chr6:15646200-15662000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr6:15647800-15662000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:15648200-15662200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr6:15648600-15662000	Weak transcription	Fetal Lung	lung
30	chr6:15648800-15662000	Weak transcription	Fetal Brain Female	brain
31	chr6:15649400-15662000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:15649600-15662000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:15649800-15662000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr6:15649800-15662000	Weak transcription	Liver	Liver
35	chr6:15649800-15662000	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr6:15649800-15662200	Weak transcription	HSMM	muscle
37	chr6:15650400-15661800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:15650800-15662000	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr6:15651000-15662000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr6:15651200-15662000	Weak transcription	Adipose Nuclei	Adipose
41	chr6:15652000-15662000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:15654200-15662000	Weak transcription	Right Atrium	heart
43	chr6:15654400-15662000	Weak transcription	Fetal Heart	heart
44	chr6:15655200-15661800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr6:15655200-15662000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:15655200-15662000	Weak transcription	Osteobl	bone
47	chr6:15655600-15662200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr6:15658200-15661800	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr6:15658200-15662000	Weak transcription	A549	lung
50	chr6:15658800-15662000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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