Variant report

Variant	nsv1027814
Chromosome Location	chr7:18144199-18194899
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:344)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:18183785-18184045	GM12878	blood:	n/a	n/a
2	BATF	chr7:18184881-18185085	GM12878	blood:	n/a	n/a
3	BATF	chr7:18184830-18185121	GM12878	blood:	n/a	n/a
4	BCL11A	chr7:18193010-18193273	GM12878	blood:	n/a	n/a
5	BRCA1	chr7:18171365-18171399	GM12878	blood:	n/a	n/a
6	CEBPB	chr7:18159690-18159890	IMR90	lung:	n/a	n/a
7	CEBPB	chr7:18181186-18181347	H1-hESC	embryonic stem cell:	n/a	chr7:18181253-18181266
8	CEBPB	chr7:18186481-18186681	A549	lung:	n/a	n/a
9	CEBPB	chr7:18186392-18186590	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPD	chr7:18163132-18163480	K562	blood:	n/a	n/a
11	CTCF	chr7:18191200-18191350	HCPEpiC	choroid plexus:	n/a	chr7:18191245-18191263 chr7:18191240-18191261
12	CTCF	chr7:18159780-18159930	HCFaa	heart:	n/a	n/a
13	CTCF	chr7:18160941-18161432	K562	blood:	n/a	n/a
14	CTCF	chr7:18191220-18191370	AoAF	blood vessel:	n/a	chr7:18191245-18191263 chr7:18191240-18191261
15	CTCF	chr7:18159700-18159850	GM12875	blood:	n/a	n/a
16	CTCF	chr7:18159674-18159980	GM12878	blood:	n/a	n/a
17	CTCF	chr7:18159800-18159950	GM12872	blood:	n/a	n/a
18	CTCF	chr7:18159760-18159910	HMF	breast:	n/a	n/a
19	CTCF	chr7:18159820-18159970	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr7:18176451-18176484	GM13976	blood:	n/a	n/a
21	CTCF	chr7:18159771-18159880	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr7:18159740-18159890	HMEC	breast:	n/a	n/a
23	CTCF	chr7:18159720-18159870	HAc	cerebellar:	n/a	n/a
24	CTCF	chr7:18159800-18159950	WI-38	lung:	n/a	n/a
25	CTCF	chr7:18159740-18159890	RPTEC	kidney:	n/a	n/a
26	CTCF	chr7:18191161-18191303	GM12878	blood:	n/a	chr7:18191245-18191263 chr7:18191240-18191261
27	CTCF	chr7:18159721-18159949	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:18159740-18159890	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr7:18191140-18191290	NHEK	skin:	n/a	chr7:18191245-18191263 chr7:18191240-18191261
30	CTCF	chr7:18159702-18159873	HepG2	liver:	n/a	n/a
31	CTCF	chr7:18159760-18159910	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr7:18191242-18191313	LNCaP	prostate:	n/a	chr7:18191245-18191263
33	CTCF	chr7:18159464-18160125	A549	lung:	n/a	n/a
34	CTCF	chr7:18191103-18191411	GM12878	blood:	n/a	chr7:18191245-18191263 chr7:18191240-18191261
35	CTCF	chr7:18159740-18159890	HPF	lung:	n/a	n/a
36	CTCF	chr7:18159720-18159870	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr7:18159760-18159910	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr7:18159740-18159890	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr7:18191152-18191291	SK-N-SH_RA	brain:	n/a	chr7:18191245-18191263 chr7:18191240-18191261
40	CTCF	chr7:18159760-18159910	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr7:18159719-18159933	NHEK	skin:	n/a	n/a
42	CTCF	chr7:18159780-18159930	BE2_C	brain:	n/a	n/a
43	CTCF	chr7:18157260-18157410	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr7:18191140-18191290	BJ	skin:	n/a	chr7:18191245-18191263 chr7:18191240-18191261
45	CTCF	chr7:18159720-18159870	HCT-116	colon:	n/a	n/a
46	CTCF	chr7:18191231-18191311	GM10248	blood:	n/a	chr7:18191245-18191263 chr7:18191240-18191261
47	CTCF	chr7:18159768-18159905	GM19238	blood:	n/a	n/a
48	CTCF	chr7:18191200-18191350	HMF	breast:	n/a	chr7:18191245-18191263 chr7:18191240-18191261
49	CTCF	chr7:18159680-18159830	GM12865	blood:	n/a	n/a
50	CTCF	chr7:18159750-18159892	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:18194528-18194578	CMK	blood:	n/a
2	chr7:18194528-18194578	ProgFib	skin:	n/a
3	chr7:18194528-18194578	NH-A	brain:	n/a
4	chr7:18194528-18194578	Hela-S3	cervix:	n/a
5	chr7:18194528-18194578	GM06990	blood:	n/a
6	chr7:18194528-18194578	SK-N-SH_RA	brain:	n/a
7	chr7:18194528-18194578	Jurkat	blood:	n/a
8	chr7:18194528-18194578	NHDF-neo	bronchial:	n/a
9	chr7:18194528-18194578	HCPEpiC	choroid plexus:	n/a
10	chr7:18194528-18194578	HCF	heart:	n/a
11	chr7:18194528-18194578	AG09309	skin:	n/a
12	chr7:18194528-18194578	GM12892	blood:	n/a
13	chr7:18194528-18194578	HUVEC	blood vessel:	n/a
14	chr7:18194528-18194578	HepG2	liver:	n/a
15	chr7:18194528-18194578	AG10803	skin:	n/a
16	chr7:18194528-18194578	SAEC	small airway:	n/a
17	chr7:18194528-18194578	U87	brain:	n/a
18	chr7:18194528-18194578	ovcar-3	ovarian:	n/a
19	chr7:18194528-18194578	AG04450	lung:	fetal
20	chr7:18194528-18194578	PrEC	prostate:	n/a
21	chr7:18194528-18194578	AoSMC	blood vessel:	n/a
22	chr7:18194528-18194578	HL-60	blood:	n/a
23	chr7:18194528-18194578	IMR90	lung:	fetal
24	chr7:18194528-18194578	LNCaP	prostate:	n/a
25	chr7:18194528-18194578	HRCEpiC	kidney:	n/a
26	chr7:18194528-18194578	Caco-2	colon:	n/a
27	chr7:18194528-18194578	PANC-1	pancreas:	n/a
28	chr7:18194528-18194578	SK-N-SH	brain:	n/a
29	chr7:18194528-18194578	GM12891	blood:	n/a
30	chr7:18194528-18194578	SK-N-MC	brain:	n/a
31	chr7:18194528-18194578	NHBE	bronchial:	n/a
32	chr7:18194528-18194578	BE2_C	brain:	n/a
33	chr7:18194528-18194578	HAEpiC	amniotic membrane:	n/a
34	chr7:18194528-18194578	PFSK-1	brain:	n/a
35	chr7:18194528-18194578	MCF-7	breast:	n/a
36	chr7:18194528-18194578	GM12878	blood:	n/a
37	chr7:18194528-18194578	HRPEpiC	eye:	n/a
38	chr7:18194528-18194578	HCM	heart:	n/a
39	chr7:18194528-18194578	HCT-116	colon:	n/a
40	chr7:18194528-18194578	HRE	kidney:	n/a
41	chr7:18194528-18194578	NT2-D1	testis:	n/a
42	chr7:18194528-18194578	MCF10A-Er-Src	breast:	n/a
43	chr7:18194528-18194578	HEEpiC	esophagus:	n/a
44	chr7:18194528-18194578	K562	blood:	n/a
45	chr7:18194528-18194578	Hepatocyte	liver:	n/a
46	chr7:18194528-18194578	BJ	skin:	n/a
47	chr7:18194528-18194578	HMEC	breast:	n/a
48	chr7:18194528-18194578	HIPEpiC	eye:	n/a
49	chr7:18194528-18194578	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:18194528-18194578	ECC-1	luminal epithelium:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:18155143..18157555-chr7:18215954..18217743,2	K562	blood:
2	chr7:18185399..18188340-chr7:18190192..18192851,2	K562	blood:
3	chr7:18162840..18165489-chr7:18245304..18246939,2	K562	blood:
4	chr7:18103601..18104557-chr7:18159371..18160090,3	MCF-7	breast:
5	chr7:18156065..18157835-chr7:18160410..18162829,3	K562	blood:
6	chr7:18156277..18159184-chr7:18161329..18163388,2	K562	blood:
7	chr7:18182937..18185828-chr7:18187655..18189338,2	K562	blood:
8	chr7:18156277..18159184-chr7:18161329..18163388,2	K562	blood:
9	chr7:17809328..17810064-chr7:18159241..18160084,2	MCF-7	breast:
10	chr5:115288586..115289484-chr7:18169519..18170041,2	MCF-7	breast:
11	chr7:18192988..18195732-chr7:18197133..18198734,2	K562	blood:
12	chr7:18182937..18185828-chr7:18187655..18189338,2	K562	blood:
13	chr7:18156065..18157835-chr7:18160410..18162829,3	K562	blood:
14	chr7:18162960..18165291-chr7:18262204..18264807,2	K562	blood:
15	chr7:18160644..18161275-chr7:18360076..18360813,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AHR-8	chr7:18191398-18191502	NONHSAT119358

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1302	chr7:18166857-18166877	MIMAT0005890_7

No data

Variant related genes	Relation type
HDAC9	TF binding region
MIR1302-6	TF binding region
HDAC9	CpG island
MIR1302-6	CpG island
ENSG00000048052	chromatin interactions

Extended variants
information (count: 1752 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1752 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34665249	chr7:18147105-18147106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538683182	chr7:18147120-18147121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553805247	chr7:18147125-18147126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149577495	chr7:18147130-18147131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576647735	chr7:18147133-18147134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572028812	chr7:18147154-18147155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74852549	chr7:18147195-18147196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566354718	chr7:18147633-18147634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182794020	chr7:18147664-18147665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs80081637	chr7:18147687-18147688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554232714	chr7:18147692-18147693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555712620	chr7:18147700-18147701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563640763	chr7:18147705-18147706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146061080	chr7:18147714-18147715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543102537	chr7:18147723-18147724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558615055	chr7:18147726-18147727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576569230	chr7:18147738-18147739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540809660	chr7:18147752-18147753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540127649	chr7:18147816-18147817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529907379	chr7:18147868-18147869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560062642	chr7:18147882-18147883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542119354	chr7:18147897-18147898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561082128	chr7:18147912-18147913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531730993	chr7:18147914-18147915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532129660	chr7:18147921-18147922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573355955	chr7:18147934-18147935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs193235373	chr7:18147942-18147943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184473330	chr7:18147957-18147958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547981743	chr7:18148036-18148037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566291368	chr7:18148062-18148063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536503592	chr7:18148063-18148064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35937844	chr7:18148075-18148076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs17138597	chr7:18148091-18148092	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs368001532	chr7:18148112-18148113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570298450	chr7:18148148-18148149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537039414	chr7:18148153-18148154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs57871121	chr7:18148184-18148185	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs576505907	chr7:18148188-18148189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540746172	chr7:18148195-18148196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552712333	chr7:18148210-18148211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574297670	chr7:18148224-18148225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541707556	chr7:18148226-18148227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10708554	chr7:18148235-18148236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs398003849	chr7:18148255-18148256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374504365	chr7:18148389-18148390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140168234	chr7:18148392-18148393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543778671	chr7:18148426-18148427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540698508	chr7:18148445-18148446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368775838	chr7:18148464-18148465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532616485	chr7:18148481-18148482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Bipolar disorder	19114987	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18147000-18147200	Enhancers	Fetal Heart	heart
2	chr7:18147600-18148800	Weak transcription	Fetal Heart	heart
3	chr7:18148800-18149800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:18148800-18149800	Enhancers	NH-A	brain
5	chr7:18148800-18150200	Enhancers	Fetal Heart	heart
6	chr7:18149000-18149600	Enhancers	NHLF	lung
7	chr7:18149200-18150000	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr7:18149400-18150000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:18149600-18150200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr7:18150000-18153000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr7:18150200-18154400	Weak transcription	Fetal Heart	heart
12	chr7:18152200-18164800	Weak transcription	Fetal Brain Male	brain
13	chr7:18153000-18153400	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr7:18153400-18153600	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr7:18153600-18153800	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr7:18153800-18155000	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr7:18154400-18154600	Enhancers	Fetal Heart	heart
18	chr7:18154600-18155000	Weak transcription	Fetal Heart	heart
19	chr7:18155000-18155600	Enhancers	Fetal Heart	heart
20	chr7:18155000-18156200	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr7:18155600-18156600	Weak transcription	Fetal Heart	heart
22	chr7:18156000-18163200	Weak transcription	Aorta	Aorta
23	chr7:18156200-18158800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr7:18156600-18156800	Enhancers	Fetal Heart	heart
25	chr7:18156800-18157200	Weak transcription	Fetal Heart	heart
26	chr7:18157200-18157600	Enhancers	Pancreas	Pancrea
27	chr7:18157200-18157800	Enhancers	Fetal Stomach	stomach
28	chr7:18157200-18161200	Enhancers	Fetal Heart	heart
29	chr7:18157400-18158000	Enhancers	NH-A	brain
30	chr7:18157600-18157800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr7:18157800-18159000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:18158000-18159000	Weak transcription	NH-A	brain
33	chr7:18158800-18159200	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr7:18159000-18159200	Enhancers	NH-A	brain
35	chr7:18159000-18159800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:18159200-18164400	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr7:18160000-18160400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:18160800-18161200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr7:18161200-18163800	Weak transcription	Fetal Heart	heart
40	chr7:18163200-18163400	Enhancers	Fetal Lung	lung
41	chr7:18163200-18163400	Enhancers	Fetal Muscle Leg	muscle
42	chr7:18163200-18163600	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr7:18163200-18163600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr7:18163200-18163600	Enhancers	Aorta	Aorta
45	chr7:18163400-18164400	Weak transcription	Fetal Lung	lung
46	chr7:18163600-18163800	Bivalent Enhancer	Aorta	Aorta
47	chr7:18163600-18165200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr7:18163800-18164800	Weak transcription	Fetal Muscle Leg	muscle
49	chr7:18163800-18165400	Weak transcription	Fetal Intestine Small	intestine
50	chr7:18163800-18169400	Enhancers	Fetal Heart	heart

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