Variant report

Variant	esv1838377
Chromosome Location	chr7:6681619-6698905
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr7:6693791-6694049	GM12878	blood:	n/a	n/a
2	BCL3	chr7:6693271-6693492	GM12878	blood:	n/a	n/a
3	BHLHE40	chr7:6698832-6699007	K562	blood:	n/a	n/a
4	BHLHE40	chr7:6685656-6685802	K562	blood:	n/a	n/a
5	BHLHE40	chr7:6698826-6699225	HepG2	liver:	n/a	n/a
6	BRCA1	chr7:6698867-6699045	H1-hESC	embryonic stem cell:	n/a	n/a
7	CCNT2	chr7:6694042-6694139	K562	blood:	n/a	n/a
8	CEBPB	chr7:6698891-6699407	HepG2	liver:	n/a	chr7:6699226-6699237
9	CHD2	chr7:6688733-6688788	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr7:6688074-6688083	MCF-7	breast:	n/a	n/a
11	CTCF	chr7:6688006-6688143	MCF-7	breast:	n/a	n/a
12	CTCF	chr7:6685100-6685250	MCF-7	breast:	n/a	n/a
13	CTCF	chr7:6687900-6688050	HMEC	breast:	n/a	n/a
14	CTCF	chr7:6687960-6688110	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr7:6688038-6688147	MCF-7	breast:	n/a	n/a
16	EGR1	chr7:6682803-6683044	K562	blood:	n/a	chr7:6682938-6682949 chr7:6682936-6682951
17	EGR1	chr7:6682837-6682995	K562	blood:	n/a	chr7:6682938-6682949 chr7:6682936-6682951
18	ELF1	chr7:6693518-6693985	GM12878	blood:	n/a	n/a
19	ELF1	chr7:6694512-6694819	GM12878	blood:	n/a	n/a
20	GABPA	chr7:6693265-6693772	H1-hESC	embryonic stem cell:	n/a	n/a
21	GABPA	chr7:6693871-6694198	H1-hESC	embryonic stem cell:	n/a	n/a
22	GATA2	chr7:6698565-6699425	SH-SY5Y	brain:	n/a	chr7:6698827-6698841
23	GATA2	chr7:6698650-6699015	HUVEC	blood vessel:	n/a	chr7:6698827-6698841
24	GATA3	chr7:6698470-6699157	SK-N-SH	brain:	n/a	n/a
25	GATA3	chr7:6698584-6699143	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr7:6698622-6699029	T-47D	breast:	n/a	n/a
27	GATA3	chr7:6698629-6699041	T-47D	breast:	n/a	n/a
28	GATA3	chr7:6698493-6698855	MCF-7	breast:	n/a	n/a
29	HMGN3	chr7:6692437-6692466	K562	blood:	n/a	n/a
30	JUND	chr7:6698789-6698954	H1-hESC	embryonic stem cell:	n/a	n/a
31	MAX	chr7:6698745-6699627	ECC-1	luminal epithelium:	n/a	chr7:6698988-6698997 chr7:6698983-6699002 chr7:6698986-6698999 chr7:6698986-6698999 chr7:6698988-6698997
32	MAX	chr7:6698619-6699703	MCF-7	breast:	n/a	chr7:6698988-6698997 chr7:6698983-6699002 chr7:6698986-6698999 chr7:6698986-6698999 chr7:6698988-6698997
33	MAX	chr7:6698806-6699141	K562	blood:	n/a	chr7:6698988-6698997 chr7:6698983-6699002 chr7:6698986-6698999 chr7:6698986-6698999 chr7:6698988-6698997
34	MAX	chr7:6698860-6699197	H1-hESC	embryonic stem cell:	n/a	chr7:6698988-6698997 chr7:6698983-6699002 chr7:6698986-6698999 chr7:6698986-6698999 chr7:6698988-6698997
35	MAX	chr7:6698710-6699513	NB4	blood:	n/a	chr7:6698988-6698997 chr7:6698983-6699002 chr7:6698986-6698999 chr7:6698986-6698999 chr7:6698988-6698997
36	MAX	chr7:6698760-6699662	ECC-1	luminal epithelium:	n/a	chr7:6698988-6698997 chr7:6698983-6699002 chr7:6698986-6698999 chr7:6698986-6698999 chr7:6698988-6698997
37	MAX	chr7:6698879-6699355	HepG2	liver:	n/a	chr7:6698988-6698997 chr7:6698983-6699002 chr7:6698986-6698999 chr7:6698986-6698999 chr7:6698988-6698997
38	MTA3	chr7:6698232-6699458	GM12878	blood:	n/a	n/a
39	MYC	chr7:6696184-6696296	MCF-7	breast:	n/a	n/a
40	MYC	chr7:6693497-6693638	MCF-7	breast:	n/a	n/a
41	MYC	chr7:6687405-6687481	MCF-7	breast:	n/a	n/a
42	MYC	chr7:6692304-6692375	MCF-7	breast:	n/a	n/a
43	NFATC1	chr7:6697463-6697790	GM12878	blood:	n/a	n/a
44	NFATC1	chr7:6698086-6698995	GM12878	blood:	n/a	n/a
45	NFYB	chr7:6696321-6696616	GM12878	blood:	n/a	chr7:6696510-6696524 chr7:6696512-6696522 chr7:6696509-6696524 chr7:6696509-6696524 chr7:6696513-6696525 chr7:6696511-6696524 chr7:6696512-6696522
46	NFYB	chr7:6696292-6696642	K562	blood:	n/a	chr7:6696510-6696524 chr7:6696512-6696522 chr7:6696509-6696524 chr7:6696509-6696524 chr7:6696513-6696525 chr7:6696511-6696524 chr7:6696512-6696522
47	PAX5	chr7:6692292-6692760	GM12878	blood:	n/a	n/a
48	PAX5	chr7:6692399-6692566	GM12878	blood:	n/a	n/a
49	PAX5	chr7:6692302-6692682	GM12878	blood:	n/a	n/a
50	PAX5	chr7:6693717-6694116	GM12891	blood:	n/a	chr7:6693933-6693952

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6694978-6695028	Hela-S3	cervix:	n/a
2	chr7:6694978-6695028	Hela-S3	cervix:	n/a
3	chr7:6695092-6695142	HUVEC	blood vessel:	n/a
4	chr7:6693838-6693888	MCF10A-Er-Src	breast:	n/a
5	chr7:6692445-6692495	U87	brain:	n/a
6	chr7:6693334-6693384	AG04450	lung:	fetal
7	chr7:6695092-6695142	H1-hESC	embryonic stem cell:	embryo
8	chr7:6690313-6690363	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:6694978-6695028	HRCEpiC	kidney:	n/a
10	chr7:6691949-6691999	HepG2	liver:	n/a
11	chr7:6690313-6690363	A549	lung:	n/a
12	chr7:6689218-6689268	NHDF-neo	bronchial:	n/a
13	chr7:6682784-6682834	AG04450	lung:	fetal
14	chr7:6693030-6693080	AG10803	skin:	n/a
15	chr7:6694373-6694423	PFSK-1	brain:	n/a
16	chr7:6695092-6695142	A549	lung:	n/a
17	chr7:6689218-6689268	K562	blood:	n/a
18	chr7:6691949-6691999	GM12891	blood:	n/a
19	chr7:6694978-6695028	MCF10A-Er-Src	breast:	n/a
20	chr7:6692445-6692495	ProgFib	skin:	n/a
21	chr7:6696120-6696170	GM19239	blood:	n/a
22	chr7:6693838-6693888	HCM	heart:	n/a
23	chr7:6692445-6692495	PANC-1	pancreas:	n/a
24	chr7:6696120-6696170	HRCEpiC	kidney:	n/a
25	chr7:6695121-6695171	HEK293	kidney:	embryo
26	chr7:6693334-6693384	GM12878	blood:	n/a
27	chr7:6694978-6695028	HMEC	breast:	n/a
28	chr7:6682784-6682834	GM12892	blood:	n/a
29	chr7:6693030-6693080	ECC-1	luminal epithelium:	n/a
30	chr7:6690313-6690363	NT2-D1	testis:	n/a
31	chr7:6682784-6682834	Hepatocyte	liver:	n/a
32	chr7:6695092-6695142	BE2_C	brain:	n/a
33	chr7:6693030-6693080	AG04450	lung:	fetal
34	chr7:6690313-6690363	H1-hESC	embryonic stem cell:	embryo
35	chr7:6690313-6690363	U87	brain:	n/a
36	chr7:6693838-6693888	NH-A	brain:	n/a
37	chr7:6682784-6682834	SK-N-SH	brain:	n/a
38	chr7:6695092-6695142	HL-60	blood:	n/a
39	chr7:6694978-6695028	U87	brain:	n/a
40	chr7:6695121-6695171	HIPEpiC	eye:	n/a
41	chr7:6682784-6682834	LNCaP	prostate:	n/a
42	chr7:6694735-6694785	Hela-S3	cervix:	n/a
43	chr7:6692445-6692495	K562	blood:	n/a
44	chr7:6693030-6693080	HMEC	breast:	n/a
45	chr7:6694978-6695028	PrEC	prostate:	n/a
46	chr7:6691949-6691999	ovcar-3	ovarian:	n/a
47	chr7:6695121-6695171	SKMC	muscle:	n/a
48	chr7:6695121-6695171	NT2-D1	testis:	n/a
49	chr7:6695092-6695142	SAEC	small airway:	n/a
50	chr7:6693334-6693384	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:6681243..6682856-chr7:6746246..6748831,2	K562	blood:
2	chr7:6698325..6700210-chr7:6703299..6704869,2	MCF-7	breast:
3	chr7:6668305..6670110-chr7:6679585..6681865,2	MCF-7	breast:
4	chr7:6689485..6692014-chr7:6722455..6725146,3	MCF-7	breast:
5	chr7:6682551..6684434-chr7:6694308..6696080,2	MCF-7	breast:
6	chr7:6688371..6689911-chr7:6696909..6698726,2	K562	blood:
7	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
8	chr7:6694849..6698438-chr7:6699530..6702045,3	K562	blood:
9	chr7:6681267..6684799-chr7:6697447..6700610,3	MCF-7	breast:
10	chr7:6685863..6688294-chr7:6688920..6690681,2	MCF-7	breast:
11	chr7:6688371..6689911-chr7:6696909..6698726,2	K562	blood:
12	chr7:6650218..6651893-chr7:6687593..6690254,2	K562	blood:
13	chr7:6692466..6696366-chr7:6696714..6698992,3	MCF-7	breast:
14	chr7:6675427..6681659-chr7:6684293..6688490,10	MCF-7	breast:
15	chr7:6674209..6679608-chr7:6682918..6689628,9	K562	blood:
16	chr7:6660093..6661828-chr7:6695492..6697100,2	MCF-7	breast:
17	chr7:6674759..6677679-chr7:6692100..6694240,3	MCF-7	breast:
18	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
19	chr7:6696313..6698315-chr7:6745284..6746997,2	K562	blood:
20	chr7:6680998..6682837-chr7:6692889..6695214,2	MCF-7	breast:
21	chr7:6680149..6683134-chr7:6689202..6690780,2	K562	blood:
22	chr7:6614762..6617092-chr7:6682142..6684739,2	K562	blood:
23	chr7:6682112..6684474-chr7:6686272..6690280,3	MCF-7	breast:
24	chr7:6627001..6634994-chr7:6673643..6681623,15	MCF-7	breast:
25	chr7:6679487..6682483-chr7:6695124..6696654,2	MCF-7	breast:
26	chr7:6675369..6676975-chr7:6698332..6700533,2	MCF-7	breast:
27	chr7:6682112..6684474-chr7:6686272..6690280,3	MCF-7	breast:
28	chr7:6668677..6671566-chr7:6683216..6685538,2	MCF-7	breast:
29	chr7:6669640..6671625-chr7:6687041..6689974,2	MCF-7	breast:
30	chr7:6685863..6688294-chr7:6688920..6690681,2	MCF-7	breast:
31	chr7:6698245..6699981-chr7:6737287..6739036,2	MCF-7	breast:
32	chr7:6683236..6686038-chr7:6768255..6771021,2	K562	blood:
33	chr7:6675838..6678415-chr7:6696567..6699140,4	MCF-7	breast:
34	chr7:6676518..6678447-chr7:6694438..6696514,2	MCF-7	breast:
35	chr7:6680998..6682837-chr7:6692889..6695214,2	MCF-7	breast:
36	chr7:6687023..6688997-chr7:6745010..6747605,2	K562	blood:
37	chr7:6672567..6674181-chr7:6688854..6690680,2	K562	blood:
38	chr7:6660564..6662217-chr7:6683757..6686361,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-2	chr7:6694495-6696063	ENSG00000260054.1

Variant related genes	Relation type
ZNF316	TF binding region
ENSG00000260054	TF binding region
ENSG00000228010	TF binding region
ZNF316	CpG island
ENSG00000260054	CpG island
ENSG00000228010	CpG island
ENSG00000136247	chromatin interactions
ENSG00000228010	chromatin interactions
ENSG00000164631	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000232581	chromatin interactions
ENSG00000260054	chromatin interactions
ENSG00000205903	chromatin interactions
ENSG00000146576	chromatin interactions

Extended variants
information (count: 798 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs940870	chr7:6681619-6681620	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538649556	chr7:6681658-6681659	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs115798817	chr7:6681660-6681661	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs569516950	chr7:6681679-6681680	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs371142400	chr7:6681682-6681683	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs186157925	chr7:6681740-6681741	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs139138466	chr7:6681742-6681743	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs573139506	chr7:6681744-6681745	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs540285762	chr7:6681746-6681747	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs190009677	chr7:6681791-6681792	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs542486363	chr7:6681811-6681812	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs544580851	chr7:6681820-6681821	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs562771917	chr7:6681865-6681866	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs200980933	chr7:6681927-6681928	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs560656325	chr7:6681932-6681933	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs542595800	chr7:6681937-6681938	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs541340917	chr7:6681938-6681939	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs561024468	chr7:6681942-6681943	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs528297003	chr7:6681987-6681988	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs546689434	chr7:6681989-6681990	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs571379366	chr7:6681995-6681996	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs79944099	chr7:6682037-6682038	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs376552997	chr7:6682046-6682047	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs568804170	chr7:6682057-6682058	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs536939901	chr7:6682064-6682065	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs561225165	chr7:6682123-6682124	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs548478329	chr7:6682152-6682153	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs544222501	chr7:6682190-6682191	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs566698996	chr7:6682201-6682202	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs534141675	chr7:6682218-6682219	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs559187393	chr7:6682222-6682223	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs576905380	chr7:6682251-6682252	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs527674086	chr7:6682252-6682253	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs538003588	chr7:6682263-6682264	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs556513013	chr7:6682317-6682318	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs574750841	chr7:6682331-6682332	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs377600054	chr7:6682357-6682358	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs542860601	chr7:6682415-6682416	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs561189224	chr7:6682424-6682425	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs367879612	chr7:6682436-6682437	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs552198441	chr7:6682447-6682448	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs564149716	chr7:6682458-6682459	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs199516430	chr7:6682474-6682475	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs573039341	chr7:6682475-6682476	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs549884593	chr7:6682494-6682495	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs540412040	chr7:6682577-6682578	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs565101763	chr7:6682581-6682582	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs532229402	chr7:6682605-6682606	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs145062142	chr7:6682607-6682608	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs148615334	chr7:6682620-6682621	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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

Chromatin state (count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6678000-6691600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:6678200-6682400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:6678200-6683200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr7:6678200-6683400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr7:6678200-6683800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr7:6678200-6684200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr7:6678200-6685000	Strong transcription	NHEK	skin
8	chr7:6678200-6698200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr7:6678400-6683000	Weak transcription	Small Intestine	intestine
10	chr7:6678400-6691600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:6678400-6691600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:6678600-6682800	Weak transcription	Stomach Mucosa	stomach
13	chr7:6678600-6687800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:6678600-6687800	Strong transcription	Fetal Intestine Large	intestine
15	chr7:6678600-6689600	Strong transcription	Fetal Intestine Small	intestine
16	chr7:6678800-6682000	Weak transcription	Psoas Muscle	Psoas
17	chr7:6678800-6685600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr7:6678800-6688600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr7:6678800-6689600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:6678800-6691200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:6678800-6691400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr7:6679000-6681800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr7:6679000-6682800	Weak transcription	Primary hematopoietic stem cells	blood
24	chr7:6679000-6684600	Strong transcription	Muscle Satellite Cultured Cells	--
25	chr7:6679000-6684800	Strong transcription	A549	lung
26	chr7:6679000-6687800	Strong transcription	Fetal Stomach	stomach
27	chr7:6679000-6689200	Strong transcription	Thymus	Thymus
28	chr7:6679000-6689400	Strong transcription	Fetal Thymus	thymus
29	chr7:6679000-6689600	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr7:6679000-6690000	Strong transcription	Fetal Brain Female	brain
31	chr7:6679000-6692200	Strong transcription	Primary T cells from cord blood	blood
32	chr7:6679000-6692600	Strong transcription	Primary B cells from peripheral blood	blood
33	chr7:6679000-6695200	Strong transcription	Stomach Smooth Muscle	stomach
34	chr7:6679000-6695400	Strong transcription	Brain Inferior Temporal Lobe	brain
35	chr7:6679200-6690200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr7:6679200-6690200	Strong transcription	Lung	lung
37	chr7:6679200-6690200	Strong transcription	NHLF	lung
38	chr7:6679200-6695400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:6679400-6682800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr7:6679400-6691600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr7:6679400-6691600	Strong transcription	Liver	Liver
42	chr7:6679400-6696400	Strong transcription	Brain Hippocampus Middle	brain
43	chr7:6679400-6703600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr7:6679600-6682800	Strong transcription	Osteobl	bone
45	chr7:6679600-6689200	Strong transcription	Brain Germinal Matrix	brain
46	chr7:6679600-6689400	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr7:6679600-6689600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr7:6679600-6693200	Strong transcription	Rectal Smooth Muscle	rectum
49	chr7:6679600-6699200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr7:6679800-6686400	Strong transcription	GM12878-XiMat	blood

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