Variant report

Variant	esv1841024
Chromosome Location	chr8:104872512-104908099
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	BATF	chr8:104876181-104876506	GM12878	blood:	n/a	n/a
2	BCL11A	chr8:104876148-104876465	GM12878	blood:	n/a	n/a
3	CTCF	chr8:104884260-104884410	SAEC	small airway:	n/a	n/a
4	CTCF	chr8:104883607-104884002	HCT-116	colon:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
5	CTCF	chr8:104883666-104883749	GM20000	blood:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
6	CTCF	chr8:104883740-104883890	HMEC	breast:	n/a	n/a
7	CTCF	chr8:104883500-104883650	GM12871	blood:	n/a	n/a
8	CTCF	chr8:104876194-104876275	MCF-7	breast:	n/a	n/a
9	CTCF	chr8:104883700-104883850	GM12868	blood:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
10	CTCF	chr8:104883720-104883870	GM12878	blood:	n/a	chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
11	CTCF	chr8:104883600-104883750	HFF	foreskin:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
12	CTCF	chr8:104883720-104883870	AG10803	skin:	n/a	chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
13	CTCF	chr8:104883620-104883770	HMF	breast:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
14	CTCF	chr8:104883680-104883830	HMEC	breast:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
15	CTCF	chr8:104883380-104883530	A549	lung:	n/a	n/a
16	CTCF	chr8:104883698-104883800	GM13976	blood:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
17	CTCF	chr8:104883660-104883821	LNCaP	prostate:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
18	CTCF	chr8:104883680-104883830	HCT-116	colon:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
19	CTCF	chr8:104883640-104883790	SK-N-SH_RA	brain:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
20	CTCF	chr8:104883618-104883919	K562	blood:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
21	CTCF	chr8:104883480-104883630	GM12865	blood:	n/a	n/a
22	CTCF	chr8:104883580-104883730	GM12864	blood:	n/a	n/a
23	CTCF	chr8:104883740-104883890	GM12869	blood:	n/a	n/a
24	CTCF	chr8:104883623-104883863	HUVEC	blood vessel:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
25	CTCF	chr8:104884220-104884370	HPF	lung:	n/a	n/a
26	CTCF	chr8:104883740-104883890	K562	blood:	n/a	n/a
27	CTCF	chr8:104883487-104883593	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:104883660-104883810	GM12873	blood:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
29	CTCF	chr8:104883680-104883830	GM12864	blood:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
30	CTCF	chr8:104884340-104884490	AG10803	skin:	n/a	n/a
31	CTCF	chr8:104883640-104883790	AG04449	skin:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
32	CTCF	chr8:104883640-104883790	HEEpiC	esophagus:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
33	CTCF	chr8:104883549-104883943	GM12878	blood:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
34	CTCF	chr8:104883700-104883850	HA-sp	spinal cord:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
35	CTCF	chr8:104883620-104883770	HUVEC	blood vessel:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
36	CTCF	chr8:104883660-104883810	HPAF	blood vessel:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
37	CTCF	chr8:104883588-104883893	IMR90	lung:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
38	CTCF	chr8:104883640-104883790	Caco-2	colon:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
39	CTCF	chr8:104883720-104883870	HRE	kidney:	n/a	chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
40	CTCF	chr8:104883668-104883826	GM12878	blood:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
41	CTCF	chr8:104884320-104884470	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr8:104883800-104883950	RPTEC	kidney:	n/a	n/a
43	CTCF	chr8:104883360-104883510	HVMF	connective:	n/a	n/a
44	CTCF	chr8:104883680-104883830	GM12867	blood:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
45	CTCF	chr8:104883554-104883840	A549	lung:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
46	CTCF	chr8:104883660-104883810	GM12865	blood:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
47	CTCF	chr8:104884220-104884370	AG09319	gingival:	n/a	n/a
48	CTCF	chr8:104884320-104884470	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr8:104883692-104883830	Pancreas_OC	pancreas:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738
50	CTCF	chr8:104883640-104883790	BJ	skin:	n/a	chr8:104883716-104883737 chr8:104883721-104883739 chr8:104883726-104883734 chr8:104883722-104883738

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:104897908-104897958	SK-N-MC	brain:	n/a
2	chr8:104897908-104897958	HepG2	liver:	n/a
3	chr8:104897908-104897958	HRCEpiC	kidney:	n/a
4	chr8:104897908-104897958	GM06990	blood:	n/a
5	chr8:104897908-104897958	HRE	kidney:	n/a
6	chr8:104897821-104897871	AG10803	skin:	n/a
7	chr8:104897821-104897871	GM19239	blood:	n/a
8	chr8:104897908-104897958	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:104897908-104897958	PFSK-1	brain:	n/a
10	chr8:104897908-104897958	HAEpiC	amniotic membrane:	n/a
11	chr8:104897908-104897958	AG04450	lung:	fetal
12	chr8:104897821-104897871	A549	lung:	n/a
13	chr8:104897821-104897871	ovcar-3	ovarian:	n/a
14	chr8:104897908-104897958	HRPEpiC	eye:	n/a
15	chr8:104897821-104897871	Hepatocyte	liver:	n/a
16	chr8:104897821-104897871	ECC-1	luminal epithelium:	n/a
17	chr8:104897908-104897958	HNPCEpiC	eye:	n/a
18	chr8:104897908-104897958	HCF	heart:	n/a
19	chr8:104897821-104897871	AoSMC	blood vessel:	n/a
20	chr8:104897821-104897871	U87	brain:	n/a
21	chr8:104897908-104897958	SAEC	small airway:	n/a
22	chr8:104897908-104897958	Hepatocyte	liver:	n/a
23	chr8:104897821-104897871	LNCaP	prostate:	n/a
24	chr8:104897908-104897958	GM19239	blood:	n/a
25	chr8:104897821-104897871	PANC-1	pancreas:	n/a
26	chr8:104897821-104897871	SK-N-MC	brain:	n/a
27	chr8:104897908-104897958	SK-N-SH	brain:	n/a
28	chr8:104897908-104897958	SKMC	muscle:	n/a
29	chr8:104897821-104897871	BE2_C	brain:	n/a
30	chr8:104897821-104897871	HCPEpiC	choroid plexus:	n/a
31	chr8:104897821-104897871	SAEC	small airway:	n/a
32	chr8:104897821-104897871	ProgFib	skin:	n/a
33	chr8:104897908-104897958	NH-A	brain:	n/a
34	chr8:104897821-104897871	HCM	heart:	n/a
35	chr8:104897821-104897871	HCT-116	colon:	n/a
36	chr8:104897908-104897958	HUVEC	blood vessel:	n/a
37	chr8:104897821-104897871	AG04450	lung:	fetal
38	chr8:104897908-104897958	T-47D	breast:	n/a
39	chr8:104897908-104897958	AG10803	skin:	n/a
40	chr8:104897821-104897871	HepG2	liver:	n/a
41	chr8:104897821-104897871	GM12878	blood:	n/a
42	chr8:104897821-104897871	T-47D	breast:	n/a
43	chr8:104897821-104897871	SK-N-SH_RA	brain:	n/a
44	chr8:104897908-104897958	LNCaP	prostate:	n/a
45	chr8:104897908-104897958	A549	lung:	n/a
46	chr8:104897908-104897958	IMR90	lung:	fetal
47	chr8:104897821-104897871	HMEC	breast:	n/a
48	chr8:104897821-104897871	HRCEpiC	kidney:	n/a
49	chr8:104897908-104897958	BJ	skin:	n/a
50	chr8:104897908-104897958	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:20694205..20697000-chr8:104874403..104876084,2	MCF-7	breast:
2	chr8:104807612..104809857-chr8:104883134..104884151,8	MCF-7	breast:
3	chr8:104719474..104720086-chr8:104883273..104884095,3	MCF-7	breast:
4	chr8:104788640..104789427-chr8:104883229..104884125,2	MCF-7	breast:
5	chr8:104720101..104721082-chr8:104883258..104883794,2	MCF-7	breast:
6	chr8:104776221..104777249-chr8:104883194..104884184,4	MCF-7	breast:

Variant related genes	Relation type
RIMS2	TF binding region
RIMS2	CpG island

Extended variants
information (count: 1246 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:1246 , 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	rs542891825	chr8:104872522-104872523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536901681	chr8:104872556-104872557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573607045	chr8:104872574-104872575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540206060	chr8:104872597-104872598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564889494	chr8:104872621-104872622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113270618	chr8:104872630-104872631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544298436	chr8:104872638-104872639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141073275	chr8:104872650-104872651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557262404	chr8:104872651-104872652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529891477	chr8:104872666-104872667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548120633	chr8:104872682-104872683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146906965	chr8:104872685-104872686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377571295	chr8:104872723-104872724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527605050	chr8:104872731-104872732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139000647	chr8:104872758-104872759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1496848	chr8:104872835-104872836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571308960	chr8:104872843-104872844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538701505	chr8:104872864-104872865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141573998	chr8:104872875-104872876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370900402	chr8:104872902-104872903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs57907696	chr8:104872911-104872912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147057872	chr8:104872967-104872968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146308911	chr8:104872969-104872970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372533806	chr8:104872976-104872977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34041732	chr8:104873017-104873018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs398086868	chr8:104873025-104873026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs398009169	chr8:104873026-104873027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573542467	chr8:104873031-104873032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534505063	chr8:104873048-104873049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs57600548	chr8:104873056-104873057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373183176	chr8:104873069-104873070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558541829	chr8:104873079-104873080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576770783	chr8:104873102-104873103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147093764	chr8:104873185-104873186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543914316	chr8:104873199-104873200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562590425	chr8:104873210-104873211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574478010	chr8:104873216-104873217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541982381	chr8:104873288-104873289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12114257	chr8:104873314-104873315	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs149296745	chr8:104873321-104873322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184724058	chr8:104873337-104873338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74873072	chr8:104873344-104873345	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
43	rs564078096	chr8:104873353-104873354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs71520858	chr8:104873394-104873395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532521003	chr8:104873399-104873400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11776873	chr8:104873436-104873437	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs530971835	chr8:104873464-104873465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188784341	chr8:104873536-104873537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371845495	chr8:104873560-104873561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181606941	chr8:104873583-104873584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104859400-104897200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:104882200-104882400	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr8:104882400-104884200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr8:104883800-104884400	Enhancers	Fetal Intestine Large	intestine
5	chr8:104883800-104885600	Enhancers	Brain Cingulate Gyrus	brain
6	chr8:104884000-104884400	Enhancers	Brain Substantia Nigra	brain
7	chr8:104884200-104885000	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr8:104885200-104885800	Enhancers	Brain Hippocampus Middle	brain
9	chr8:104885600-104886600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr8:104885600-104886800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr8:104886400-104887200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr8:104886400-104887200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:104886400-104887200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr8:104886400-104887200	Enhancers	HMEC	breast
15	chr8:104886400-104887200	Enhancers	NHEK	skin
16	chr8:104886600-104886800	Enhancers	Brain Cingulate Gyrus	brain
17	chr8:104887200-104890000	Weak transcription	HMEC	breast
18	chr8:104887200-104891200	Weak transcription	NHEK	skin
19	chr8:104889800-104890400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:104890000-104890600	Enhancers	HMEC	breast
21	chr8:104890200-104891000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:104890600-104891000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:104890600-104891200	Weak transcription	HMEC	breast
24	chr8:104891200-104891400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr8:104891200-104891400	Enhancers	HMEC	breast
26	chr8:104891200-104891400	Enhancers	NHEK	skin
27	chr8:104891400-104897600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr8:104895800-104897600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:104896600-104900000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr8:104896800-104898200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr8:104897000-104897600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr8:104897200-104898200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr8:104897200-104914200	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr8:104897400-104897800	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr8:104897600-104898200	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr8:104897600-104898400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr8:104897600-104899400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr8:104897800-104898000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
39	chr8:104898000-104898400	Strong transcription	Pancreatic Islets	Pancreatic Islet
40	chr8:104898200-104900400	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr8:104898200-104919000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:104898400-104902400	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr8:104899400-104933400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:104901200-104902000	Enhancers	Brain Anterior Caudate	brain
45	chr8:104902000-104902400	Flanking Active TSS	Brain Anterior Caudate	brain
46	chr8:104902000-104902600	Enhancers	Brain Hippocampus Middle	brain
47	chr8:104902200-104903400	Enhancers	Fetal Brain Male	brain
48	chr8:104902400-104902600	Enhancers	Brain Anterior Caudate	brain
49	chr8:104902400-104902800	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr8:104905600-104906200	Enhancers	Fetal Intestine Large	intestine

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