Variant report

Variant	esv3340228
Chromosome Location	chr7:6702427-6704975
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	BACH1	chr7:6703886-6703996	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr7:6703432-6703706	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr7:6702828-6702909	GM20000	blood:	n/a	n/a
4	CTCF	chr7:6704080-6704230	GM12866	blood:	n/a	n/a
5	E2F6	chr7:6703347-6704662	H1-hESC	embryonic stem cell:	n/a	chr7:6703521-6703530 chr7:6703910-6703919 chr7:6703696-6703705
6	EGR1	chr7:6703418-6703972	ECC-1	luminal epithelium:	n/a	chr7:6703788-6703801 chr7:6703516-6703529 chr7:6703788-6703802 chr7:6703515-6703530 chr7:6703788-6703801 chr7:6703777-6703790 chr7:6703521-6703531 chr7:6703516-6703530 chr7:6703516-6703529 chr7:6703519-6703528 chr7:6703516-6703529 chr7:6703788-6703801 chr7:6703791-6703800 chr7:6703519-6703529 chr7:6703787-6703802 chr7:6703788-6703801
7	EGR1	chr7:6703445-6703933	H1-hESC	embryonic stem cell:	n/a	chr7:6703788-6703801 chr7:6703516-6703529 chr7:6703788-6703802 chr7:6703515-6703530 chr7:6703788-6703801 chr7:6703777-6703790 chr7:6703521-6703531 chr7:6703516-6703530 chr7:6703516-6703529 chr7:6703519-6703528 chr7:6703516-6703529 chr7:6703788-6703801 chr7:6703791-6703800 chr7:6703519-6703529 chr7:6703787-6703802 chr7:6703788-6703801
8	EGR1	chr7:6703567-6704000	ECC-1	luminal epithelium:	n/a	chr7:6703788-6703801 chr7:6703788-6703802 chr7:6703788-6703801 chr7:6703777-6703790 chr7:6703788-6703801 chr7:6703791-6703800 chr7:6703787-6703802 chr7:6703788-6703801
9	GTF2F1	chr7:6703575-6703765	H1-hESC	embryonic stem cell:	n/a	n/a
10	JUND	chr7:6703496-6703785	H1-hESC	embryonic stem cell:	n/a	n/a
11	MAX	chr7:6703434-6704298	ECC-1	luminal epithelium:	n/a	chr7:6703943-6703952
12	MAX	chr7:6703369-6704307	H1-hESC	embryonic stem cell:	n/a	chr7:6703943-6703952
13	MYC	chr7:6703437-6703695	H1-hESC	embryonic stem cell:	n/a	n/a
14	NRF1	chr7:6703441-6703787	H1-hESC	embryonic stem cell:	n/a	chr7:6703696-6703705 chr7:6703521-6703530 chr7:6703698-6703707
15	NRF1	chr7:6703300-6703914	SK-N-SH	brain:	n/a	chr7:6703696-6703705 chr7:6703521-6703530 chr7:6703698-6703707
16	POLR2A	chr7:6703441-6703895	ECC-1	luminal epithelium:	n/a	n/a
17	POLR2A	chr7:6704397-6704714	K562	blood:	n/a	n/a
18	POLR2A	chr7:6703453-6703852	H1-neurons	neurons:	n/a	n/a
19	POLR2A	chr7:6703457-6703764	SK-N-SH	brain:	n/a	n/a
20	POLR2A	chr7:6704944-6704946	K562	blood:	n/a	n/a
21	POLR2A	chr7:6703323-6704459	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr7:6703423-6703783	SK-N-MC	brain:	n/a	n/a
23	POLR2A	chr7:6703471-6704307	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr7:6703537-6703640	HUVEC	blood vessel:	n/a	n/a
25	POLR2A	chr7:6703488-6704102	ECC-1	luminal epithelium:	n/a	n/a
26	POLR2A	chr7:6703525-6703697	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr7:6703464-6703772	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr7:6703466-6703765	H1-hESC	embryonic stem cell:	n/a	n/a
29	REST	chr7:6704020-6704170	H1-hESC	embryonic stem cell:	n/a	n/a
30	REST	chr7:6703953-6704190	SK-N-SH	brain:	n/a	n/a
31	SIN3A	chr7:6703712-6704177	H1-hESC	embryonic stem cell:	n/a	chr7:6703769-6703778
32	SP1	chr7:6703418-6703769	H1-hESC	embryonic stem cell:	n/a	chr7:6703520-6703532 chr7:6703551-6703562 chr7:6703521-6703530 chr7:6703522-6703531 chr7:6703540-6703549 chr7:6703521-6703531 chr7:6703539-6703551 chr7:6703522-6703531 chr7:6703521-6703531 chr7:6703540-6703549 chr7:6703541-6703550 chr7:6703520-6703532
33	SP1	chr7:6703437-6703746	H1-hESC	embryonic stem cell:	n/a	chr7:6703520-6703532 chr7:6703551-6703562 chr7:6703521-6703530 chr7:6703522-6703531 chr7:6703540-6703549 chr7:6703521-6703531 chr7:6703539-6703551 chr7:6703522-6703531 chr7:6703521-6703531 chr7:6703540-6703549 chr7:6703541-6703550 chr7:6703520-6703532
34	SP4	chr7:6703418-6703777	H1-hESC	embryonic stem cell:	n/a	chr7:6703551-6703562 chr7:6703518-6703534 chr7:6703516-6703532
35	SP4	chr7:6703413-6703779	H1-hESC	embryonic stem cell:	n/a	chr7:6703551-6703562 chr7:6703518-6703534 chr7:6703516-6703532
36	TAF1	chr7:6703426-6703824	ECC-1	luminal epithelium:	n/a	n/a
37	TAF1	chr7:6703429-6703806	H1-hESC	embryonic stem cell:	n/a	n/a
38	TAF1	chr7:6703426-6703662	SK-N-SH	brain:	n/a	n/a
39	TAF1	chr7:6703394-6703829	H1-hESC	embryonic stem cell:	n/a	n/a
40	TAF7	chr7:6703477-6703832	H1-hESC	embryonic stem cell:	n/a	n/a
41	TBP	chr7:6703462-6703783	H1-hESC	embryonic stem cell:	n/a	n/a
42	TBP	chr7:6704096-6704413	H1-hESC	embryonic stem cell:	n/a	n/a
43	ZBTB7A	chr7:6703262-6704111	ECC-1	luminal epithelium:	n/a	n/a
44	ZBTB7A	chr7:6703455-6704066	ECC-1	luminal epithelium:	n/a	n/a
45	ZNF143	chr7:6703631-6704230	H1-hESC	embryonic stem cell:	n/a	chr7:6703696-6703706

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6704074-6704124	PrEC	prostate:	n/a
2	chr7:6704194-6704244	U87	brain:	n/a
3	chr7:6702706-6702756	ECC-1	luminal epithelium:	n/a
4	chr7:6703533-6703583	A549	lung:	n/a
5	chr7:6703533-6703583	AG04449	skin:	fetal
6	chr7:6702706-6702756	GM12892	blood:	n/a
7	chr7:6703803-6703853	HMEC	breast:	n/a
8	chr7:6704045-6704095	SAEC	small airway:	n/a
9	chr7:6704074-6704124	SK-N-SH_RA	brain:	n/a
10	chr7:6703708-6703758	GM12878	blood:	n/a
11	chr7:6704194-6704244	NHBE	bronchial:	n/a
12	chr7:6703533-6703583	HRPEpiC	eye:	n/a
13	chr7:6703533-6703583	U87	brain:	n/a
14	chr7:6704045-6704095	AoSMC	blood vessel:	n/a
15	chr7:6704074-6704124	HEK293	kidney:	embryo
16	chr7:6703803-6703853	HCT-116	colon:	n/a
17	chr7:6703533-6703583	SK-N-SH	brain:	n/a
18	chr7:6703533-6703583	HRCEpiC	kidney:	n/a
19	chr7:6703533-6703583	LNCaP	prostate:	n/a
20	chr7:6704074-6704124	AG09309	skin:	n/a
21	chr7:6704194-6704244	MCF-7	breast:	n/a
22	chr7:6704074-6704124	Hela-S3	cervix:	n/a
23	chr7:6704194-6704244	T-47D	breast:	n/a
24	chr7:6703708-6703758	NH-A	brain:	n/a
25	chr7:6703708-6703758	CMK	blood:	n/a
26	chr7:6703533-6703583	IMR90	lung:	fetal
27	chr7:6703708-6703758	LNCaP	prostate:	n/a
28	chr7:6704045-6704095	SK-N-MC	brain:	n/a
29	chr7:6702706-6702756	HL-60	blood:	n/a
30	chr7:6703533-6703583	MCF10A-Er-Src	breast:	n/a
31	chr7:6703803-6703853	PFSK-1	brain:	n/a
32	chr7:6703803-6703853	RPTEC	kidney:	n/a
33	chr7:6704194-6704244	GM19239	blood:	n/a
34	chr7:6703533-6703583	K562	blood:	n/a
35	chr7:6704045-6704095	U87	brain:	n/a
36	chr7:6704074-6704124	MCF10A-Er-Src	breast:	n/a
37	chr7:6703533-6703583	NHDF-neo	bronchial:	n/a
38	chr7:6703803-6703853	ProgFib	skin:	n/a
39	chr7:6704194-6704244	HRE	kidney:	n/a
40	chr7:6704045-6704095	SK-N-SH_RA	brain:	n/a
41	chr7:6703803-6703853	HRCEpiC	kidney:	n/a
42	chr7:6704194-6704244	RPTEC	kidney:	n/a
43	chr7:6704045-6704095	NT2-D1	testis:	n/a
44	chr7:6704045-6704095	Hepatocyte	liver:	n/a
45	chr7:6703708-6703758	HepG2	liver:	n/a
46	chr7:6703803-6703853	SK-N-SH_RA	brain:	n/a
47	chr7:6704074-6704124	NB4	blood:	n/a
48	chr7:6704045-6704095	A549	lung:	n/a
49	chr7:6704045-6704095	HRPEpiC	eye:	n/a
50	chr7:6702706-6702756	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:6700299..6703221-chr7:6744305..6746051,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-1	chr7:6704675-6704739	NONHSAT119055
2	lnc-AC073343.1-1	chr7:6703605-6703674	ENSG00000228010.1
3	lnc-AC073343.1-1	chr7:6704675-6704739	ENSG00000228010.1
4	lnc-AC073343.1-1	chr7:6704675-6704739	ENSG00000228010.1
5	lnc-AC073343.1-1	chr7:6703605-6703674	NONHSAT119055
6	lnc-AC073343.1-1	chr7:6704675-6705152	ENSG00000228010.1
7	lnc-AC073343.1-1	chr7:6704675-6705152	NONHSAT119056
8	lnc-AC073343.1-1	chr7:6703605-6703674	NONHSAT119056
9	lnc-AC073343.1-1	chr7:6703605-6703674	ENSG00000228010.1
10	lnc-AC073343.1-1	chr7:6703605-6703674	ENSG00000228010.1

Variant related genes	Relation type
ENSG00000228010	TF binding region
ENSG00000228010	CpG island

Extended variants
information (count: 110 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551384903	chr7:6702435-6702436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570250725	chr7:6702447-6702448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553457191	chr7:6702470-6702471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148751917	chr7:6702502-6702503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549263607	chr7:6702511-6702512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111836446	chr7:6702514-6702515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534758944	chr7:6702516-6702517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190573559	chr7:6702539-6702540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571433082	chr7:6702545-6702546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538642035	chr7:6702567-6702568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539200361	chr7:6702705-6702706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148784955	chr7:6702769-6702770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367634026	chr7:6702789-6702790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554552770	chr7:6702790-6702791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576220325	chr7:6702791-6702792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs62439673	chr7:6702843-6702844	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs113305995	chr7:6702860-6702861	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs147887726	chr7:6702864-6702865	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs541263816	chr7:6702870-6702871	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs386709838	chr7:6702930-6702931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375671610	chr7:6702931-6702932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139856709	chr7:6702932-6702933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563298191	chr7:6702939-6702940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117745042	chr7:6702951-6702952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549664892	chr7:6702958-6702959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561240342	chr7:6702972-6702973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564405157	chr7:6703005-6703006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528638515	chr7:6703008-6703009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576497496	chr7:6703010-6703011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546835165	chr7:6703085-6703086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184479367	chr7:6703087-6703088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539135218	chr7:6703109-6703110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550655813	chr7:6703122-6703123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569257677	chr7:6703128-6703129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536915303	chr7:6703183-6703184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189698410	chr7:6703311-6703312	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs555621873	chr7:6703431-6703432	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs181342591	chr7:6703526-6703527	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs574012523	chr7:6703648-6703649	Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs534808616	chr7:6703659-6703660	Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs553244848	chr7:6703684-6703685	Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs145471039	chr7:6703690-6703691	Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545111021	chr7:6703773-6703774	Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs151054009	chr7:6703822-6703823	Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
45	rs528709905	chr7:6703824-6703825	Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
46	rs375493997	chr7:6703828-6703829	Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
47	rs113463409	chr7:6703832-6703833	Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
48	rs572538729	chr7:6703835-6703836	Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
49	rs368838759	chr7:6703843-6703844	Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs2464879	chr7:6703846-6703847	Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6679400-6703600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr7:6691000-6703400	Weak transcription	Colon Smooth Muscle	Colon
3	chr7:6692600-6703400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr7:6694800-6703600	Weak transcription	Aorta	Aorta
5	chr7:6695000-6703400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr7:6695000-6703400	Weak transcription	Dnd41	blood
7	chr7:6695200-6703400	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr7:6695200-6703400	Weak transcription	Left Ventricle	heart
9	chr7:6695200-6703400	Weak transcription	Thymus	Thymus
10	chr7:6695200-6703600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr7:6695200-6703600	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr7:6695400-6703400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr7:6695400-6703400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr7:6695400-6703400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr7:6695400-6703600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr7:6695400-6703600	Weak transcription	NHLF	lung
17	chr7:6695600-6703400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr7:6695600-6704000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr7:6696000-6703400	Weak transcription	Spleen	Spleen
20	chr7:6696400-6703400	Weak transcription	Ovary	ovary
21	chr7:6696600-6703800	Weak transcription	Primary T cells from cord blood	blood
22	chr7:6699200-6703400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr7:6699200-6703400	Weak transcription	Right Atrium	heart
24	chr7:6699200-6703600	Weak transcription	Primary hematopoietic stem cells	blood
25	chr7:6699200-6703600	Weak transcription	Pancreas	Pancrea
26	chr7:6699400-6703400	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr7:6699400-6703400	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr7:6699400-6703400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:6699400-6703400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr7:6699400-6703400	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr7:6699400-6703400	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr7:6699400-6703400	Weak transcription	Brain Hippocampus Middle	brain
33	chr7:6699400-6703400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr7:6699400-6703400	Weak transcription	Brain Substantia Nigra	brain
35	chr7:6699400-6703400	Weak transcription	Esophagus	oesophagus
36	chr7:6699400-6703400	Weak transcription	Lung	lung
37	chr7:6699400-6703400	Weak transcription	Right Ventricle	heart
38	chr7:6699400-6703600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:6699400-6703600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr7:6699400-6703600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr7:6699400-6704000	Weak transcription	Fetal Intestine Large	intestine
42	chr7:6699600-6703000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:6699600-6703400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr7:6699600-6703400	Weak transcription	Brain Cingulate Gyrus	brain
45	chr7:6699600-6703600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr7:6702000-6703600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:6702400-6703400	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr7:6702800-6703200	Weak transcription	Brain Anterior Caudate	brain
49	chr7:6703000-6703400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:6703200-6704800	Enhancers	Fetal Brain Male	brain

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