Variant report

Variant	nsv887968
Chromosome Location	chr7:39123165-39198960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:207)
CpG islands
(count:490)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:207 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:39170789-39170985	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:39123997-39124380	HepG2	liver:	n/a	n/a
3	ATF1	chr7:39166728-39166972	K562	blood:	n/a	n/a
4	BACH1	chr7:39141948-39142050	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr7:39126332-39126513	K562	blood:	n/a	n/a
6	BRCA1	chr7:39169846-39169849	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr7:39151534-39151679	K562	blood:	n/a	n/a
8	CEBPB	chr7:39177694-39177706	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:39156676-39156890	HepG2	liver:	n/a	chr7:39156759-39156770
10	CEBPB	chr7:39165607-39165698	IMR90	lung:	n/a	chr7:39165664-39165675
11	CEBPB	chr7:39136485-39136628	HepG2	liver:	n/a	chr7:39136524-39136533 chr7:39136522-39136533 chr7:39136522-39136535
12	CEBPB	chr7:39156678-39156896	A549	lung:	n/a	chr7:39156759-39156770
13	CEBPB	chr7:39165529-39165845	K562	blood:	n/a	chr7:39165664-39165675
14	CEBPB	chr7:39165562-39165784	H1-hESC	embryonic stem cell:	n/a	chr7:39165664-39165675
15	CEBPB	chr7:39156673-39156868	IMR90	lung:	n/a	chr7:39156759-39156770
16	CEBPB	chr7:39165570-39165788	HepG2	liver:	n/a	chr7:39165664-39165675
17	CEBPB	chr7:39165516-39165800	K562	blood:	n/a	chr7:39165664-39165675
18	CEBPB	chr7:39175580-39175779	HepG2	liver:	n/a	chr7:39175672-39175683
19	CEBPB	chr7:39170784-39171080	HepG2	liver:	n/a	chr7:39170874-39170885 chr7:39170930-39170941 chr7:39170930-39170943 chr7:39170932-39170943 chr7:39170930-39170943
20	CEBPB	chr7:39170880-39171061	K562	blood:	n/a	chr7:39170930-39170941 chr7:39170930-39170943 chr7:39170932-39170943 chr7:39170930-39170943
21	CEBPZ	chr7:39174103-39174179	HepG2	liver:	n/a	n/a
22	CTCF	chr7:39193340-39193490	AG04450	lung:	n/a	n/a
23	CTCF	chr7:39193300-39193450	GM12865	blood:	n/a	n/a
24	CTCF	chr7:39128457-39128505	K562	blood:	n/a	n/a
25	CTCF	chr7:39180100-39180250	GM12874	blood:	n/a	n/a
26	CTCF	chr7:39193360-39193510	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr7:39138840-39138989	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:39188600-39188750	SAEC	small airway:	n/a	n/a
29	CTCF	chr7:39173052-39173078	GM13976	blood:	n/a	n/a
30	CTCF	chr7:39128451-39128565	Medullo	brain:	n/a	n/a
31	CTCF	chr7:39193345-39193529	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr7:39128444-39128563	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:39193411-39193477	A549	lung:	n/a	n/a
34	CTCF	chr7:39193360-39193510	GM12873	blood:	n/a	n/a
35	CTCF	chr7:39138496-39138515	GM13976	blood:	n/a	n/a
36	CTCF	chr7:39193260-39193410	GM12873	blood:	n/a	n/a
37	CTCF	chr7:39193380-39193530	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:39193286-39193638	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:39128532-39128541	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr7:39193367-39193491	K562	blood:	n/a	n/a
41	CTCF	chr7:39193260-39193410	BE2_C	brain:	n/a	n/a
42	CTCF	chr7:39193300-39193450	HepG2	liver:	n/a	n/a
43	CTCF	chr7:39193260-39193410	A549	lung:	n/a	n/a
44	CTCF	chr7:39193373-39193511	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:39155240-39155390	GM06990	blood:	n/a	n/a
46	CTCF	chr7:39138849-39138988	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:39193370-39193509	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:39193320-39193470	HCT-116	colon:	n/a	n/a
49	CTCF	chr7:39193345-39193498	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:39193374-39193502	MCF-7	breast:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:39171034-39171084	HL-60	blood:	n/a
2	chr7:39171113-39171163	AG09319	gingival:	n/a
3	chr7:39171034-39171084	HL-60	blood:	n/a
4	chr7:39171113-39171163	AG09319	gingival:	n/a
5	chr7:39126804-39126854	ovcar-3	ovarian:	n/a
6	chr7:39170539-39170589	AG04449	skin:	fetal
7	chr7:39126804-39126854	GM12891	blood:	n/a
8	chr7:39171070-39171120	BE2_C	brain:	n/a
9	chr7:39170497-39170547	H1-hESC	embryonic stem cell:	embryo
10	chr7:39170497-39170547	HCT-116	colon:	n/a
11	chr7:39170763-39170813	HL-60	blood:	n/a
12	chr7:39125198-39125248	NB4	blood:	n/a
13	chr7:39170539-39170589	HMEC	breast:	n/a
14	chr7:39170539-39170589	HRCEpiC	kidney:	n/a
15	chr7:39170763-39170813	PANC-1	pancreas:	n/a
16	chr7:39126804-39126854	AG04450	lung:	fetal
17	chr7:39171113-39171163	ovcar-3	ovarian:	n/a
18	chr7:39171034-39171084	SK-N-MC	brain:	n/a
19	chr7:39125198-39125248	HCM	heart:	n/a
20	chr7:39126804-39126854	BE2_C	brain:	n/a
21	chr7:39126804-39126854	NHDF-neo	bronchial:	n/a
22	chr7:39170539-39170589	HL-60	blood:	n/a
23	chr7:39170539-39170589	HCM	heart:	n/a
24	chr7:39170763-39170813	NT2-D1	testis:	n/a
25	chr7:39125198-39125248	ovcar-3	ovarian:	n/a
26	chr7:39125198-39125248	SKMC	muscle:	n/a
27	chr7:39170539-39170589	BJ	skin:	n/a
28	chr7:39126804-39126854	NHBE	bronchial:	n/a
29	chr7:39170763-39170813	HRE	kidney:	n/a
30	chr7:39170497-39170547	HAEpiC	amniotic membrane:	n/a
31	chr7:39170539-39170589	HRE	kidney:	n/a
32	chr7:39126804-39126854	ECC-1	luminal epithelium:	n/a
33	chr7:39126804-39126854	PANC-1	pancreas:	n/a
34	chr7:39171070-39171120	HEK293	kidney:	embryo
35	chr7:39171034-39171084	MCF-7	breast:	n/a
36	chr7:39170497-39170547	MCF10A-Er-Src	breast:	n/a
37	chr7:39125198-39125248	HepG2	liver:	n/a
38	chr7:39171070-39171120	HAEpiC	amniotic membrane:	n/a
39	chr7:39171070-39171120	GM12892	blood:	n/a
40	chr7:39171113-39171163	A549	lung:	n/a
41	chr7:39125198-39125248	HRPEpiC	eye:	n/a
42	chr7:39126804-39126854	U87	brain:	n/a
43	chr7:39171034-39171084	HRE	kidney:	n/a
44	chr7:39171070-39171120	BJ	skin:	n/a
45	chr7:39170763-39170813	HAEpiC	amniotic membrane:	n/a
46	chr7:39171034-39171084	AoSMC	blood vessel:	n/a
47	chr7:39170763-39170813	HUVEC	blood vessel:	n/a
48	chr7:39171070-39171120	GM12878	blood:	n/a
49	chr7:39170539-39170589	AG10803	skin:	n/a
50	chr7:39171113-39171163	K562	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:39137033..39139788-chr7:39144579..39146603,2	K562	blood:
2	chr7:39191469..39193442-chr7:39196110..39198005,2	K562	blood:
3	chr7:39155263..39157100-chr7:39158946..39161624,2	K562	blood:
4	chr7:39196101..39198199-chr7:39208525..39210124,2	K562	blood:
5	chr7:39181307..39183603-chr7:39185314..39187095,2	MCF-7	breast:
6	chr7:39127870..39129771-chr7:39130949..39133880,2	K562	blood:
7	chr7:39195274..39197700-chr7:39206282..39208251,3	K562	blood:
8	chr7:39127870..39129771-chr7:39130949..39133880,2	K562	blood:
9	chr7:39181307..39183603-chr7:39185314..39187095,2	MCF-7	breast:
10	chr7:39118345..39121127-chr7:39144193..39146924,2	K562	blood:
11	chr7:39138311..39140874-chr7:39175563..39178454,2	K562	blood:
12	chr7:39155263..39157100-chr7:39158946..39161624,2	K562	blood:
13	chr7:39191469..39193442-chr7:39196110..39198005,2	K562	blood:
14	chr7:39137033..39139788-chr7:39144579..39146603,2	K562	blood:
15	chr7:39198600..39200599-chr7:39202951..39205373,2	K562	blood:
16	chr7:39138311..39140874-chr7:39175563..39178454,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-YAE1D1-3	chr7:39160433-39160502	NONHSAT120198
2	lnc-YAE1D1-3	chr7:39171978-39172246	NONHSAT120198
3	lnc-YAE1D1-3	chr7:39125461-39125631	NONHSAT120198

No data

Variant related genes	Relation type
POU6F2	TF binding region
POU6F2	CpG island

Extended variants
information (count: 1240 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1240 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6959715	chr7:39123165-39123166	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370451599	chr7:39123225-39123226	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs16880005	chr7:39123257-39123258	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs181429806	chr7:39123265-39123266	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs376730416	chr7:39123285-39123286	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs572299899	chr7:39123324-39123325	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs17171531	chr7:39123325-39123326	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs368368140	chr7:39123426-39123427	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs2177799	chr7:39123438-39123439	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs111998962	chr7:39123509-39123510	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs564029369	chr7:39123531-39123532	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs532972413	chr7:39123622-39123623	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs116327115	chr7:39123627-39123628	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs371166237	chr7:39123642-39123643	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs563350113	chr7:39123648-39123649	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs530934654	chr7:39123652-39123653	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs141552061	chr7:39123688-39123689	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs150908034	chr7:39123693-39123694	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs568609506	chr7:39123699-39123700	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs535172711	chr7:39123714-39123715	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs534460779	chr7:39123780-39123781	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs36065581	chr7:39123852-39123853	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs570480533	chr7:39123975-39123976	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs539472850	chr7:39123996-39123997	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs185962558	chr7:39124021-39124022	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs77220763	chr7:39124042-39124043	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs576116571	chr7:39124043-39124044	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs190610313	chr7:39124058-39124059	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs570502617	chr7:39124073-39124074	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs79756471	chr7:39124101-39124102	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs182477731	chr7:39124105-39124106	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs543855152	chr7:39124195-39124196	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs185637169	chr7:39124215-39124216	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs375307372	chr7:39124216-39124217	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs564393007	chr7:39124283-39124284	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs78116367	chr7:39124314-39124315	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs190592150	chr7:39124339-39124340	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs182884525	chr7:39124363-39124364	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs10254198	chr7:39124375-39124376	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs368083463	chr7:39124420-39124421	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs17171532	chr7:39124426-39124427	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs372094597	chr7:39124461-39124462	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs73373258	chr7:39124500-39124501	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs562270962	chr7:39124501-39124502	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs527897336	chr7:39124586-39124587	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs188636851	chr7:39124661-39124662	Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs570791020	chr7:39124664-39124665	Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs576305872	chr7:39124669-39124670	Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs193274866	chr7:39124691-39124692	Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs17431633	chr7:39124704-39124705	Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39113600-39123400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:39115600-39125200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr7:39120400-39123600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:39121400-39123200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:39122000-39123400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr7:39122400-39124000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:39122600-39125000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:39122800-39123200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr7:39122800-39125000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr7:39123000-39124400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr7:39123200-39124400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
12	chr7:39123200-39124800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:39123200-39125000	Enhancers	Fetal Brain Male	brain
14	chr7:39123400-39123600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:39123400-39123800	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr7:39123400-39124400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr7:39123600-39124400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:39123600-39125000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr7:39123800-39126600	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr7:39124000-39124200	Bivalent Enhancer	Fetal Kidney	kidney
21	chr7:39124000-39124800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr7:39124000-39125000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr7:39124200-39124600	Enhancers	Fetal Brain Female	brain
24	chr7:39124200-39125000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr7:39124400-39124600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr7:39124400-39124600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
27	chr7:39124400-39124600	Active TSS	Brain Inferior Temporal Lobe	brain
28	chr7:39124400-39124800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr7:39124400-39124800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
30	chr7:39124400-39125000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:39124400-39125200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:39124400-39125200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr7:39124400-39125800	Active TSS	Brain Cingulate Gyrus	brain
34	chr7:39124600-39125000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr7:39124600-39125200	Flanking Active TSS	Fetal Brain Female	brain
36	chr7:39124600-39125400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
37	chr7:39124600-39125400	Enhancers	Fetal Heart	heart
38	chr7:39124600-39126000	Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr7:39124800-39125000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr7:39124800-39125000	Enhancers	Primary hematopoietic stem cells	blood
41	chr7:39124800-39125000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr7:39124800-39125000	Active TSS	Brain Angular Gyrus	brain
43	chr7:39124800-39125000	Enhancers	Brain Germinal Matrix	brain
44	chr7:39124800-39125200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
45	chr7:39124800-39125200	Active TSS	Brain Anterior Caudate	brain
46	chr7:39124800-39125200	Active TSS	Psoas Muscle	Psoas
47	chr7:39124800-39125400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr7:39124800-39125600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:39124800-39125600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr7:39124800-39126000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell

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