Variant report

Variant	esv1834684
Chromosome Location	chr7:6671496-6721661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1337)
CpG islands
(count:2260)
Chromatin interactive
region (count:90)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1337 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6680032-6680221	K562	blood:	n/a	n/a
2	ATF2	chr7:6676670-6676974	GM12878	blood:	n/a	n/a
3	ATF3	chr7:6679904-6680092	K562	blood:	n/a	n/a
4	ATF3	chr7:6676663-6677108	GM12878	blood:	n/a	n/a
5	ATF3	chr7:6676764-6677038	K562	blood:	n/a	n/a
6	ATF3	chr7:6676729-6677016	HepG2	liver:	n/a	n/a
7	ATF3	chr7:6676775-6677020	GM12878	blood:	n/a	n/a
8	BACH1	chr7:6676690-6676978	K562	blood:	n/a	n/a
9	BACH1	chr7:6676413-6677735	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:6677373-6677430	K562	blood:	n/a	n/a
11	BACH1	chr7:6703886-6703996	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr7:6679547-6679737	GM12878	blood:	n/a	n/a
13	BCL3	chr7:6693791-6694049	GM12878	blood:	n/a	n/a
14	BCL3	chr7:6676620-6677051	GM12878	blood:	n/a	chr7:6676897-6676906
15	BCL3	chr7:6693271-6693492	GM12878	blood:	n/a	n/a
16	BCLAF1	chr7:6676612-6677075	GM12878	blood:	n/a	chr7:6676897-6676906
17	BHLHE40	chr7:6698832-6699007	K562	blood:	n/a	n/a
18	BHLHE40	chr7:6679828-6680319	K562	blood:	n/a	n/a
19	BHLHE40	chr7:6676405-6676427	K562	blood:	n/a	n/a
20	BHLHE40	chr7:6676643-6677601	GM12878	blood:	n/a	chr7:6677407-6677423
21	BHLHE40	chr7:6698826-6699225	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:6679587-6679733	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:6685656-6685802	K562	blood:	n/a	n/a
24	BHLHE40	chr7:6676722-6677023	K562	blood:	n/a	n/a
25	BHLHE40	chr7:6677264-6677647	K562	blood:	n/a	chr7:6677407-6677423
26	BRCA1	chr7:6698867-6699045	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr7:6715451-6715881	K562	blood:	n/a	n/a
28	CBX3	chr7:6677286-6677693	K562	blood:	n/a	n/a
29	CBX3	chr7:6676642-6676930	K562	blood:	n/a	n/a
30	CBX3	chr7:6679776-6680216	K562	blood:	n/a	n/a
31	CBX3	chr7:6714585-6714947	K562	blood:	n/a	n/a
32	CBX3	chr7:6679531-6680589	K562	blood:	n/a	n/a
33	CBX3	chr7:6715528-6715998	K562	blood:	n/a	n/a
34	CCNT2	chr7:6676308-6677623	K562	blood:	n/a	n/a
35	CCNT2	chr7:6694042-6694139	K562	blood:	n/a	n/a
36	CEBPB	chr7:6698987-6699470	MCF-7	breast:	n/a	chr7:6699226-6699237
37	CEBPB	chr7:6699089-6699426	H1-hESC	embryonic stem cell:	n/a	chr7:6699226-6699237
38	CEBPB	chr7:6679441-6679533	K562	blood:	n/a	n/a
39	CEBPB	chr7:6698891-6699407	HepG2	liver:	n/a	chr7:6699226-6699237
40	CEBPB	chr7:6699157-6699396	Hela-S3	cervix:	n/a	chr7:6699226-6699237
41	CEBPB	chr7:6679964-6680434	K562	blood:	n/a	n/a
42	CEBPB	chr7:6679421-6679645	A549	lung:	n/a	n/a
43	CEBPB	chr7:6699039-6699442	ECC-1	luminal epithelium:	n/a	chr7:6699226-6699237
44	CEBPB	chr7:6679892-6680277	K562	blood:	n/a	n/a
45	CEBPB	chr7:6699127-6699332	HepG2	liver:	n/a	chr7:6699226-6699237
46	CEBPB	chr7:6698995-6699540	ECC-1	luminal epithelium:	n/a	chr7:6699226-6699237
47	CEBPB	chr7:6699055-6699407	HepG2	liver:	n/a	chr7:6699226-6699237
48	CEBPB	chr7:6679380-6679580	HepG2	liver:	n/a	n/a
49	CEBPD	chr7:6676750-6677014	HepG2	liver:	n/a	n/a
50	CEBPD	chr7:6676694-6677135	HepG2	liver:	n/a	n/a

(count:2260 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6677433-6677483	AG10803	skin:	n/a
2	chr7:6677606-6677656	HEEpiC	esophagus:	n/a
3	chr7:6693838-6693888	Hepatocyte	liver:	n/a
4	chr7:6677433-6677483	AG10803	skin:	n/a
5	chr7:6677606-6677656	HEEpiC	esophagus:	n/a
6	chr7:6693838-6693888	Hepatocyte	liver:	n/a
7	chr7:6676168-6676218	SAEC	small airway:	n/a
8	chr7:6703533-6703583	NHBE	bronchial:	n/a
9	chr7:6676784-6676834	BE2_C	brain:	n/a
10	chr7:6677433-6677483	NH-A	brain:	n/a
11	chr7:6695092-6695142	BJ	skin:	n/a
12	chr7:6698992-6699042	AG04450	lung:	fetal
13	chr7:6696120-6696170	HAEpiC	amniotic membrane:	n/a
14	chr7:6674031-6674081	HepG2	liver:	n/a
15	chr7:6704045-6704095	BE2_C	brain:	n/a
16	chr7:6677494-6677544	AG09309	skin:	n/a
17	chr7:6703533-6703583	HNPCEpiC	eye:	n/a
18	chr7:6677606-6677656	HAEpiC	amniotic membrane:	n/a
19	chr7:6676630-6676680	GM12891	blood:	n/a
20	chr7:6693838-6693888	HNPCEpiC	eye:	n/a
21	chr7:6703533-6703583	SK-N-SH	brain:	n/a
22	chr7:6676001-6676051	U87	brain:	n/a
23	chr7:6693838-6693888	Hela-S3	cervix:	n/a
24	chr7:6682784-6682834	U87	brain:	n/a
25	chr7:6695092-6695142	SK-N-SH	brain:	n/a
26	chr7:6681379-6681429	HepG2	liver:	n/a
27	chr7:6707858-6707908	Hepatocyte	liver:	n/a
28	chr7:6690313-6690363	MCF10A-Er-Src	breast:	n/a
29	chr7:6702706-6702756	A549	lung:	n/a
30	chr7:6690313-6690363	U87	brain:	n/a
31	chr7:6694735-6694785	AG09319	gingival:	n/a
32	chr7:6698992-6699042	AoSMC	blood vessel:	n/a
33	chr7:6695121-6695171	PFSK-1	brain:	n/a
34	chr7:6690313-6690363	GM12891	blood:	n/a
35	chr7:6703803-6703853	ProgFib	skin:	n/a
36	chr7:6704074-6704124	SKMC	muscle:	n/a
37	chr7:6704045-6704095	H1-hESC	embryonic stem cell:	embryo
38	chr7:6698992-6699042	NHBE	bronchial:	n/a
39	chr7:6692445-6692495	AoSMC	blood vessel:	n/a
40	chr7:6694978-6695028	HCF	heart:	n/a
41	chr7:6693334-6693384	NHDF-neo	bronchial:	n/a
42	chr7:6703533-6703583	A549	lung:	n/a
43	chr7:6694373-6694423	GM12892	blood:	n/a
44	chr7:6704045-6704095	SKMC	muscle:	n/a
45	chr7:6699526-6699576	Hela-S3	cervix:	n/a
46	chr7:6704045-6704095	NT2-D1	testis:	n/a
47	chr7:6703708-6703758	BE2_C	brain:	n/a
48	chr7:6681379-6681429	AG04449	skin:	fetal
49	chr7:6677433-6677483	H1-hESC	embryonic stem cell:	embryo
50	chr7:6682784-6682834	HL-60	blood:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:6706877..6708740-chr7:6715302..6717943,2	K562	blood:
2	chr7:6645170..6647656-chr7:6721647..6723270,2	K562	blood:
3	chr7:6694849..6698438-chr7:6699530..6702045,3	K562	blood:
4	chr7:6681267..6684799-chr7:6697447..6700610,3	MCF-7	breast:
5	chr7:6715674..6717325-chr7:6724359..6726574,2	K562	blood:
6	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
7	chr17:57920745..57921576-chr7:6676970..6677850,2	HCT-116	colon:
8	chr7:6628215..6631115-chr7:6675239..6679126,9	MCF-7	breast:
9	chr7:6700100..6701879-chr7:6709660..6714552,4	MCF-7	breast:
10	chr7:6629079..6630175-chr7:6676992..6678000,4	MCF-7	breast:
11	chr7:6641654..6643210-chr7:6674814..6676517,2	MCF-7	breast:
12	chr7:6715429..6717492-chr7:6718379..6720782,3	K562	blood:
13	chr7:6675962..6678642-chr7:6744432..6748032,4	MCF-7	breast:
14	chr7:6688371..6689911-chr7:6696909..6698726,2	K562	blood:
15	chr7:6720927..6723913-chr7:6737715..6740062,2	K562	blood:
16	chr7:6718119..6720452-chr7:6726209..6729204,2	K562	blood:
17	chr7:6676193..6679067-chr7:6744810..6746794,4	K562	blood:
18	chr7:6641830..6642345-chr7:6698974..6699620,2	MCF-7	breast:
19	chr7:6692466..6696366-chr7:6696714..6698992,3	MCF-7	breast:
20	chr7:6660564..6662217-chr7:6683757..6686361,2	MCF-7	breast:
21	chr12:56510812..56512603-chr7:6677169..6678802,2	MCF-7	breast:
22	chr7:6680149..6683134-chr7:6689202..6690780,2	K562	blood:
23	chr7:6650218..6651893-chr7:6687593..6690254,2	K562	blood:
24	chr7:6676568..6678542-chr7:6699146..6700802,2	MCF-7	breast:
25	chr7:6541950..6543739-chr7:6677071..6679453,2	K562	blood:
26	chr7:6713296..6716134-chr7:6731301..6732830,2	MCF-7	breast:
27	chr7:6682112..6684474-chr7:6686272..6690280,3	MCF-7	breast:
28	chr7:6675427..6681659-chr7:6684293..6688490,10	MCF-7	breast:
29	chr7:6682112..6684474-chr7:6686272..6690280,3	MCF-7	breast:
30	chr7:6696313..6698315-chr7:6745284..6746997,2	K562	blood:
31	chr7:6669640..6671625-chr7:6687041..6689974,2	MCF-7	breast:
32	chr7:6614762..6617092-chr7:6682142..6684739,2	K562	blood:
33	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
34	chr7:6682551..6684434-chr7:6694308..6696080,2	MCF-7	breast:
35	chr7:6675369..6676975-chr7:6698332..6700533,2	MCF-7	breast:
36	chr7:6702535..6704854-chr7:6706365..6710112,3	K562	blood:
37	chr7:6668677..6671566-chr7:6683216..6685538,2	MCF-7	breast:
38	chr7:6676518..6678447-chr7:6694438..6696514,2	MCF-7	breast:
39	chr7:6680998..6682837-chr7:6692889..6695214,2	MCF-7	breast:
40	chr10:104155341..104155841-chr7:6676464..6677005,2	Hela-S3	cervix:
41	chr7:6668305..6670110-chr7:6679585..6681865,2	MCF-7	breast:
42	chr7:6700299..6703221-chr7:6744305..6746051,2	MCF-7	breast:
43	chr7:6683236..6686038-chr7:6768255..6771021,2	K562	blood:
44	chr7:6685863..6688294-chr7:6688920..6690681,2	MCF-7	breast:
45	chr7:6674759..6677679-chr7:6692100..6694240,3	MCF-7	breast:
46	chr7:6629033..6631170-chr7:6716133..6717693,2	K562	blood:
47	chr7:6716360..6719322-chr7:6721448..6722993,2	K562	blood:
48	chr7:6698245..6699981-chr7:6737287..6739036,2	MCF-7	breast:
49	chr7:6720927..6724330-chr7:6736281..6739215,3	K562	blood:
50	chr7:6666562..6671587-chr7:6674314..6680724,9	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-1	chr7:6703605-6703674	NONHSAT119055
2	lnc-AC073343.1-2	chr7:6694495-6696063	ENSG00000260054.1
3	lnc-AC073343.1-1	chr7:6703605-6703674	ENSG00000228010.1
4	lnc-AC073343.1-1	chr7:6712836-6714110	NONHSAT119055
5	lnc-AC073343.1-1	chr7:6712836-6713398	NONHSAT119056
6	lnc-AC073343.1-3	chr7:6717086-6718009	NONHSAT119057
7	lnc-AC073343.1-1	chr7:6703605-6703674	ENSG00000228010.1
8	lnc-ZNF12-1	chr7:6708412-6708689	expReg_chr7_763_-
9	lnc-AC073343.1-1	chr7:6704675-6704739	ENSG00000228010.1
10	lnc-AC073343.1-1	chr7:6703605-6703674	NONHSAT119056
11	lnc-AC073343.1-1	chr7:6704675-6705152	NONHSAT119056
12	lnc-ZNF853-2	chr7:6679361-6680635	ucscGeneNc_uc003sqr_1
13	lnc-AC073343.1-1	chr7:6704675-6704739	NONHSAT119055
14	lnc-AC073343.1-1	chr7:6703605-6703674	ENSG00000228010.1
15	lnc-AC073343.1-1	chr7:6704675-6705152	ENSG00000228010.1
16	lnc-AC073343.1-1	chr7:6704675-6704739	ENSG00000228010.1
17	lnc-AC073343.1-1	chr7:6712836-6713232	ENSG00000228010.1

No data

Variant related genes	Relation type
ENSG00000198580	TF binding region
ZNF316	TF binding region
ENSG00000260054	TF binding region
ENSG00000228010	TF binding region
ENSG00000198580	CpG island
ZNF316	CpG island
ENSG00000260054	CpG island
ENSG00000228010	CpG island
ENSG00000146576	chromatin interactions
ENSG00000260054	chromatin interactions
ENSG00000164631	chromatin interactions
ENSG00000136240	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000205903	chromatin interactions
ENSG00000077150	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000215045	chromatin interactions
ENSG00000198580	chromatin interactions
ENSG00000265245	chromatin interactions
ENSG00000228010	chromatin interactions
ENSG00000269781	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000236609	chromatin interactions
ENSG00000232581	chromatin interactions

Extended variants
information (count: 2573 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2573 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2140905	chr7:6671496-6671497	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150890666	chr7:6671506-6671507	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs184658936	chr7:6671536-6671537	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs556336523	chr7:6671619-6671620	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs535248297	chr7:6671620-6671621	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs117647375	chr7:6671690-6671691	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs571955970	chr7:6671700-6671701	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs554257947	chr7:6671715-6671716	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs572324244	chr7:6671720-6671721	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs189498311	chr7:6671722-6671723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs563283353	chr7:6671723-6671724	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs140074873	chr7:6671781-6671782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs532440607	chr7:6671794-6671795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs530674680	chr7:6671798-6671799	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs375840061	chr7:6671816-6671817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs529927013	chr7:6671886-6671887	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs144133564	chr7:6671892-6671893	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs62441324	chr7:6671907-6671908	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs113158916	chr7:6671942-6671943	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs527251341	chr7:6671956-6671957	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373714234	chr7:6671960-6671961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs34998745	chr7:6672035-6672036	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs79202623	chr7:6672036-6672037	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs557351397	chr7:6672043-6672044	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs147320517	chr7:6672079-6672080	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs570159199	chr7:6672104-6672105	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538128084	chr7:6672111-6672112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs180770900	chr7:6672128-6672129	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536718579	chr7:6672180-6672181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs568280564	chr7:6672212-6672213	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs555076537	chr7:6672213-6672214	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs140737445	chr7:6672230-6672231	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs149763506	chr7:6672264-6672265	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371493614	chr7:6672269-6672270	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs546023343	chr7:6672273-6672274	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185218519	chr7:6672281-6672282	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs576539597	chr7:6672308-6672309	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs191294740	chr7:6672309-6672310	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs115417312	chr7:6672316-6672317	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181358474	chr7:6672365-6672366	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs6961782	chr7:6672379-6672380	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs560128795	chr7:6672391-6672392	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148521176	chr7:6672398-6672399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs552015817	chr7:6672400-6672401	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs369496501	chr7:6672406-6672407	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs568144905	chr7:6672410-6672411	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs34830975	chr7:6672411-6672412	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570099060	chr7:6672412-6672413	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs531221988	chr7:6672421-6672422	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs550033366	chr7:6672438-6672439	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1789 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6656000-6676000	Weak transcription	Psoas Muscle	Psoas
2	chr7:6656200-6675800	Weak transcription	HSMM	muscle
3	chr7:6656800-6675800	Weak transcription	Fetal Brain Male	brain
4	chr7:6660200-6676000	Weak transcription	Colonic Mucosa	Colon
5	chr7:6661800-6675800	Weak transcription	Pancreas	Pancrea
6	chr7:6661800-6676000	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr7:6661800-6676200	Weak transcription	Right Atrium	heart
8	chr7:6662800-6676000	Weak transcription	Colon Smooth Muscle	Colon
9	chr7:6663200-6676000	Weak transcription	Brain Anterior Caudate	brain
10	chr7:6663200-6676000	Weak transcription	Rectal Smooth Muscle	rectum
11	chr7:6663800-6676000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:6663800-6676000	Weak transcription	Brain Angular Gyrus	brain
13	chr7:6663800-6676000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr7:6663800-6676000	Weak transcription	Brain Substantia Nigra	brain
15	chr7:6663800-6676000	Weak transcription	Fetal Intestine Large	intestine
16	chr7:6663800-6676000	Weak transcription	Gastric	stomach
17	chr7:6663800-6676000	Weak transcription	Left Ventricle	heart
18	chr7:6663800-6676000	Weak transcription	Lung	lung
19	chr7:6663800-6676000	Weak transcription	Right Ventricle	heart
20	chr7:6663800-6676000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr7:6664000-6675800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr7:6664000-6676000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr7:6664200-6676000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:6664200-6676000	Weak transcription	Ovary	ovary
25	chr7:6664400-6675200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr7:6664400-6676000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:6665200-6675800	Weak transcription	Stomach Smooth Muscle	stomach
28	chr7:6665200-6676000	Weak transcription	Brain Germinal Matrix	brain
29	chr7:6665400-6675800	Weak transcription	Fetal Lung	lung
30	chr7:6665400-6675800	Weak transcription	Fetal Muscle Leg	muscle
31	chr7:6665400-6676000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr7:6665400-6676000	Weak transcription	Brain Hippocampus Middle	brain
33	chr7:6665600-6675800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:6665600-6676000	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr7:6666000-6676000	Weak transcription	Fetal Brain Female	brain
36	chr7:6668200-6675200	Weak transcription	Spleen	Spleen
37	chr7:6669600-6671800	Enhancers	Esophagus	oesophagus
38	chr7:6670200-6675200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:6670400-6674000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:6670400-6676000	Weak transcription	Fetal Intestine Small	intestine
41	chr7:6670600-6676000	Weak transcription	Placenta	Placenta
42	chr7:6671400-6671600	Enhancers	Fetal Thymus	thymus
43	chr7:6671400-6672000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:6671800-6675200	Weak transcription	Esophagus	oesophagus
45	chr7:6671800-6675800	Weak transcription	HMEC	breast
46	chr7:6672000-6676000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr7:6673200-6674000	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr7:6673400-6673600	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr7:6673400-6675000	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr7:6673600-6673800	Enhancers	Fetal Muscle Trunk	muscle

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