Variant report

Variant	nsv887809
Chromosome Location	chr7:18089306-18150005
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	ARID3A	chr7:18121390-18121560	K562	blood:	n/a	n/a
2	BACH1	chr7:18125731-18126123	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:18126908-18127068	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:18128064-18128069	K562	blood:	n/a	n/a
5	BHLHE40	chr7:18133764-18133769	K562	blood:	n/a	n/a
6	BRCA1	chr7:18126101-18126108	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr7:18121275-18121562	K562	blood:	n/a	n/a
8	CBX3	chr7:18121316-18121579	K562	blood:	n/a	n/a
9	CCNT2	chr7:18125916-18126441	K562	blood:	n/a	n/a
10	CEBPB	chr7:18092535-18093052	IMR90	lung:	n/a	chr7:18092646-18092659 chr7:18092648-18092659 chr7:18092646-18092657
11	CEBPB	chr7:18137658-18137944	HepG2	liver:	n/a	chr7:18137852-18137865 chr7:18137775-18137786
12	CEBPB	chr7:18140895-18141159	A549	lung:	n/a	chr7:18141039-18141050
13	CEBPB	chr7:18115062-18115328	A549	lung:	n/a	chr7:18115178-18115189
14	CEBPB	chr7:18104194-18104393	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:18104259-18104421	A549	lung:	n/a	n/a
16	CEBPB	chr7:18115123-18115292	HepG2	liver:	n/a	chr7:18115178-18115189
17	CEBPB	chr7:18102134-18102374	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:18104029-18104369	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr7:18092550-18093150	A549	lung:	n/a	chr7:18092646-18092659 chr7:18092648-18092659 chr7:18092646-18092657
20	CEBPB	chr7:18104111-18104400	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:18092472-18093105	K562	blood:	n/a	chr7:18092646-18092659 chr7:18092648-18092659 chr7:18092646-18092657
22	CEBPB	chr7:18140889-18141184	HepG2	liver:	n/a	chr7:18141039-18141050
23	CEBPB	chr7:18092547-18093153	Hela-S3	cervix:	n/a	chr7:18092646-18092659 chr7:18092648-18092659 chr7:18092646-18092657
24	CEBPB	chr7:18092478-18093189	HepG2	liver:	n/a	chr7:18092646-18092659 chr7:18092648-18092659 chr7:18092646-18092657
25	CHD1	chr7:18126956-18127037	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr7:18126859-18127082	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr7:18126743-18126924	Hela-S3	cervix:	n/a	n/a
28	CREB1	chr7:18126141-18126426	A549	lung:	n/a	n/a
29	CTCF	chr7:18103960-18104110	GM12875	blood:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
30	CTCF	chr7:18125920-18126070	GM12868	blood:	n/a	n/a
31	CTCF	chr7:18103960-18104110	WERI-Rb-1	eye:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
32	CTCF	chr7:18096120-18096270	A549	lung:	n/a	n/a
33	CTCF	chr7:18103980-18104130	WERI-Rb-1	eye:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
34	CTCF	chr7:18103945-18104177	LNCaP	prostate:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
35	CTCF	chr7:18104000-18104150	HRPEpiC	eye:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
36	CTCF	chr7:18103980-18104130	HCFaa	heart:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
37	CTCF	chr7:18103960-18104110	BJ	skin:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
38	CTCF	chr7:18126762-18126824	A549	lung:	n/a	n/a
39	CTCF	chr7:18103980-18104130	BE2_C	brain:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
40	CTCF	chr7:18103980-18104130	GM12875	blood:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
41	CTCF	chr7:18102940-18103090	NB4	blood:	n/a	n/a
42	CTCF	chr7:18103864-18104243	H1-hESC	embryonic stem cell:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
43	CTCF	chr7:18103980-18104130	HAc	cerebellar:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
44	CTCF	chr7:18125860-18126010	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:18104040-18104190	HCT-116	colon:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
46	CTCF	chr7:18104020-18104170	GM12864	blood:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
47	CTCF	chr7:18125840-18125990	HCM	heart:	n/a	n/a
48	CTCF	chr7:18103940-18104090	NHLF	lung:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
49	CTCF	chr7:18103980-18104130	GM12878	blood:	n/a	chr7:18104063-18104076 chr7:18104060-18104078
50	CTCF	chr7:18103952-18104129	A549	lung:	n/a	chr7:18104063-18104076 chr7:18104060-18104078

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:18127112-18127162	HIPEpiC	eye:	n/a
2	chr7:18127112-18127162	HIPEpiC	eye:	n/a
3	chr7:18126459-18126509	Hepatocyte	liver:	n/a
4	chr7:18126902-18126952	HPAEpiC	pulmonary alveolar:	n/a
5	chr7:18127503-18127553	NHDF-neo	bronchial:	n/a
6	chr7:18126473-18126523	HAEpiC	amniotic membrane:	n/a
7	chr7:18126473-18126523	IMR90	lung:	fetal
8	chr7:18127029-18127079	H1-hESC	embryonic stem cell:	embryo
9	chr7:18126070-18126120	SK-N-SH	brain:	n/a
10	chr7:18126473-18126523	HCM	heart:	n/a
11	chr7:18127029-18127079	GM06990	blood:	n/a
12	chr7:18127503-18127553	HAEpiC	amniotic membrane:	n/a
13	chr7:18126902-18126952	NT2-D1	testis:	n/a
14	chr7:18127029-18127079	HCPEpiC	choroid plexus:	n/a
15	chr7:18121961-18122011	T-47D	breast:	n/a
16	chr7:18127112-18127162	HRE	kidney:	n/a
17	chr7:18127112-18127162	HNPCEpiC	eye:	n/a
18	chr7:18125881-18125931	ECC-1	luminal epithelium:	n/a
19	chr7:18127468-18127518	HCPEpiC	choroid plexus:	n/a
20	chr7:18126070-18126120	SKMC	muscle:	n/a
21	chr7:18127112-18127162	HEEpiC	esophagus:	n/a
22	chr7:18127503-18127553	GM19239	blood:	n/a
23	chr7:18126070-18126120	HRPEpiC	eye:	n/a
24	chr7:18125881-18125931	HEK293	kidney:	embryo
25	chr7:18121961-18122011	HL-60	blood:	n/a
26	chr7:18126902-18126952	HEEpiC	esophagus:	n/a
27	chr7:18126902-18126952	AG09309	skin:	n/a
28	chr7:18127112-18127162	SK-N-MC	brain:	n/a
29	chr7:18126473-18126523	NT2-D1	testis:	n/a
30	chr7:18127029-18127079	NHDF-neo	bronchial:	n/a
31	chr7:18130344-18130394	PANC-1	pancreas:	n/a
32	chr7:18127503-18127553	ovcar-3	ovarian:	n/a
33	chr7:18127029-18127079	NHBE	bronchial:	n/a
34	chr7:18126070-18126120	ovcar-3	ovarian:	n/a
35	chr7:18125881-18125931	HUVEC	blood vessel:	n/a
36	chr7:18127112-18127162	NHDF-neo	bronchial:	n/a
37	chr7:18130344-18130394	AG04450	lung:	fetal
38	chr7:18127029-18127079	ECC-1	luminal epithelium:	n/a
39	chr7:18127029-18127079	Caco-2	colon:	n/a
40	chr7:18121961-18122011	ovcar-3	ovarian:	n/a
41	chr7:18126473-18126523	HEK293	kidney:	embryo
42	chr7:18127112-18127162	PANC-1	pancreas:	n/a
43	chr7:18127029-18127079	NT2-D1	testis:	n/a
44	chr7:18126459-18126509	CMK	blood:	n/a
45	chr7:18126070-18126120	SAEC	small airway:	n/a
46	chr7:18126994-18127044	AG10803	skin:	n/a
47	chr7:18127112-18127162	HMEC	breast:	n/a
48	chr7:18130344-18130394	HRPEpiC	eye:	n/a
49	chr7:18127468-18127518	PrEC	prostate:	n/a
50	chr7:18130344-18130394	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:18103601..18104557-chr7:18159371..18160090,3	MCF-7	breast:
2	chr7:18122391..18124419-chr7:18124842..18127391,3	K562	blood:
3	chr7:18135277..18137845-chr7:18140738..18142358,2	K562	blood:
4	chr7:18086835..18088605-chr7:18090406..18092394,2	K562	blood:
5	chr7:18083618..18086351-chr7:18088635..18091366,2	K562	blood:
6	chr7:18133911..18137845-chr7:18139797..18142475,5	K562	blood:
7	chr7:18135277..18137845-chr7:18140738..18142358,2	K562	blood:
8	chr7:18103570..18104553-chr7:18385072..18385885,2	MCF-7	breast:
9	chr7:18122372..18124419-chr7:18124842..18127391,3	K562	blood:
10	chr7:18133911..18137845-chr7:18139797..18142475,5	K562	blood:
11	chr7:17979679..17981563-chr7:18126378..18128454,2	MCF-7	breast:
12	chr7:18083711..18086360-chr7:18089871..18092747,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AHR-8	chr7:18127506-18127658	NONHSAT119356

Variant related genes	Relation type
HDAC9	TF binding region
HDAC9	CpG island
ENSG00000048052	chromatin interactions
ENSG00000071189	chromatin interactions

Extended variants
information (count: 997 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:997 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4721691	chr7:18089306-18089307	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76891185	chr7:18089351-18089352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35394355	chr7:18089361-18089362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76688312	chr7:18089389-18089390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142434802	chr7:18089405-18089406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs137915197	chr7:18089422-18089423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538779310	chr7:18089442-18089443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181605120	chr7:18089460-18089461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544076382	chr7:18089477-18089478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142461251	chr7:18089514-18089515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532735609	chr7:18089519-18089520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150080487	chr7:18089640-18089641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111964442	chr7:18089680-18089681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558481655	chr7:18089690-18089691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530170092	chr7:18089697-18089698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186634763	chr7:18089710-18089711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138391313	chr7:18089735-18089736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537785686	chr7:18089745-18089746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376200356	chr7:18089793-18089794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149254669	chr7:18089826-18089827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571399890	chr7:18089853-18089854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144591438	chr7:18089878-18089879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553513394	chr7:18089921-18089922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190777780	chr7:18089988-18089989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182014479	chr7:18089994-18089995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554175785	chr7:18089999-18090000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs386710864	chr7:18090004-18090005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs62446957	chr7:18090009-18090010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76651491	chr7:18090012-18090013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565561628	chr7:18090019-18090020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373202536	chr7:18090047-18090048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370772772	chr7:18090064-18090065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186276485	chr7:18090126-18090127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189682109	chr7:18090137-18090138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182080105	chr7:18090185-18090186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566159174	chr7:18090186-18090187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554280003	chr7:18090198-18090199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185491652	chr7:18090239-18090240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548687113	chr7:18090251-18090252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs10257697	chr7:18090280-18090281	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs111939108	chr7:18090288-18090289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12673112	chr7:18090317-18090318	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs139816889	chr7:18090353-18090354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571529520	chr7:18090371-18090372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554399176	chr7:18090389-18090390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572627079	chr7:18090486-18090487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538502089	chr7:18090488-18090489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577479534	chr7:18090560-18090561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79014142	chr7:18090583-18090584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112060351	chr7:18090606-18090607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Melanoma	18172304	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
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	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
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18080200-18092800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:18090000-18091000	Enhancers	Fetal Heart	heart
3	chr7:18091000-18095000	Weak transcription	Fetal Heart	heart
4	chr7:18092400-18093600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr7:18092800-18093200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:18095000-18095400	Enhancers	Fetal Heart	heart
7	chr7:18095400-18095800	Flanking Active TSS	Fetal Heart	heart
8	chr7:18095800-18096000	Enhancers	Fetal Heart	heart
9	chr7:18098400-18099200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:18098600-18099000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr7:18098600-18099000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr7:18098600-18099000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr7:18098600-18099200	Enhancers	H9 Cell Line	embryonic stem cell
14	chr7:18098600-18099200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:18102000-18102600	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr7:18107400-18107600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:18122000-18122400	ZNF genes & repeats	Pancreas	Pancrea
18	chr7:18122400-18125600	Weak transcription	Pancreas	Pancrea
19	chr7:18124400-18125000	Enhancers	Fetal Heart	heart
20	chr7:18125000-18125200	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr7:18125000-18125800	Flanking Active TSS	Fetal Heart	heart
22	chr7:18125200-18125400	Enhancers	Brain Angular Gyrus	brain
23	chr7:18125200-18125400	Enhancers	Brain Germinal Matrix	brain
24	chr7:18125200-18125400	Flanking Active TSS	Colon Smooth Muscle	Colon
25	chr7:18125200-18125600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:18125200-18125600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr7:18125200-18125800	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
28	chr7:18125200-18127600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
29	chr7:18125200-18128000	Active TSS	Brain Inferior Temporal Lobe	brain
30	chr7:18125400-18125600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:18125400-18125600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
32	chr7:18125400-18125600	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
33	chr7:18125400-18125600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr7:18125400-18125600	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr7:18125400-18125600	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr7:18125400-18125600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr7:18125400-18125600	Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr7:18125400-18125600	Bivalent Enhancer	Fetal Kidney	kidney
39	chr7:18125400-18125600	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
40	chr7:18125400-18125600	Active TSS	Stomach Smooth Muscle	stomach
41	chr7:18125400-18125600	Enhancers	A549	lung
42	chr7:18125400-18125600	Enhancers	HUVEC	blood vessel
43	chr7:18125400-18125800	Flanking Active TSS	Brain Angular Gyrus	brain
44	chr7:18125400-18126000	Flanking Active TSS	Brain Germinal Matrix	brain
45	chr7:18125400-18126000	Bivalent Enhancer	Fetal Lung	lung
46	chr7:18125400-18126800	Active TSS	Colon Smooth Muscle	Colon
47	chr7:18125400-18127000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
48	chr7:18125400-18127000	Active TSS	Fetal Brain Male	brain
49	chr7:18125400-18127000	Active TSS	Fetal Brain Female	brain
50	chr7:18125400-18127600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell

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