Variant report

Variant	esv3493283
Chromosome Location	chr9:100784615-100805700
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	chr9:100797107-100797256	K562	blood:	n/a	n/a
2	ATF2	chr9:100796914-100797400	GM12878	blood:	n/a	n/a
3	ATF2	chr9:100801870-100802389	GM12878	blood:	n/a	n/a
4	ATF2	chr9:100797428-100798370	GM12878	blood:	n/a	n/a
5	ATF2	chr9:100797142-100798288	GM12878	blood:	n/a	n/a
6	BATF	chr9:100797958-100798263	GM12878	blood:	n/a	n/a
7	BATF	chr9:100801838-100802383	GM12878	blood:	n/a	n/a
8	BATF	chr9:100801939-100802311	GM12878	blood:	n/a	n/a
9	BATF	chr9:100801373-100801701	GM12878	blood:	n/a	n/a
10	BATF	chr9:100798032-100798263	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:100801947-100802297	GM12878	blood:	n/a	n/a
12	BCL11A	chr9:100798027-100798264	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:100797837-100798277	GM12878	blood:	n/a	n/a
14	BCL3	chr9:100797832-100798277	GM12878	blood:	n/a	n/a
15	BCLAF1	chr9:100801178-100801689	GM12878	blood:	n/a	n/a
16	BCLAF1	chr9:100796947-100797720	GM12878	blood:	n/a	n/a
17	BCLAF1	chr9:100797827-100798374	GM12878	blood:	n/a	n/a
18	BCLAF1	chr9:100797467-100798266	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:100797080-100797713	GM12878	blood:	n/a	n/a
20	BHLHE40	chr9:100802048-100802400	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:100797914-100798224	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:100797033-100797270	K562	blood:	n/a	n/a
23	BRCA1	chr9:100796922-100797162	HepG2	liver:	n/a	n/a
24	CBX3	chr9:100796926-100797390	K562	blood:	n/a	n/a
25	CCNT2	chr9:100797116-100797311	K562	blood:	n/a	n/a
26	CEBPB	chr9:100797992-100798399	IMR90	lung:	n/a	n/a
27	CEBPB	chr9:100794286-100794621	IMR90	lung:	n/a	n/a
28	CHD1	chr9:100797125-100798006	GM12878	blood:	n/a	n/a
29	CHD1	chr9:100801844-100801893	GM12878	blood:	n/a	n/a
30	CHD2	chr9:100797116-100797283	HepG2	liver:	n/a	n/a
31	CHD2	chr9:100797023-100797265	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr9:100797540-100798192	GM12878	blood:	n/a	n/a
33	CREB1	chr9:100796952-100797382	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr9:100801340-100801490	GM12875	blood:	n/a	n/a
35	CTCF	chr9:100797042-100797341	LNCaP	prostate:	n/a	chr9:100797184-100797194 chr9:100797187-100797196 chr9:100797181-100797199 chr9:100797182-100797198 chr9:100797176-100797197 chr9:100797183-100797196
36	CTCF	chr9:100797120-100797270	GM12868	blood:	n/a	chr9:100797184-100797194 chr9:100797187-100797196 chr9:100797181-100797199 chr9:100797182-100797198 chr9:100797176-100797197 chr9:100797183-100797196
37	CTCF	chr9:100797100-100797250	HL-60	blood:	n/a	chr9:100797184-100797194 chr9:100797187-100797196 chr9:100797181-100797199 chr9:100797182-100797198 chr9:100797176-100797197 chr9:100797183-100797196
38	CTCF	chr9:100797120-100797270	BE2_C	brain:	n/a	chr9:100797184-100797194 chr9:100797187-100797196 chr9:100797181-100797199 chr9:100797182-100797198 chr9:100797176-100797197 chr9:100797183-100797196
39	CTCF	chr9:100797120-100797270	HUVEC	blood vessel:	n/a	chr9:100797184-100797194 chr9:100797187-100797196 chr9:100797181-100797199 chr9:100797182-100797198 chr9:100797176-100797197 chr9:100797183-100797196
40	CTCF	chr9:100796995-100797349	GM12892	blood:	n/a	chr9:100797184-100797194 chr9:100797187-100797196 chr9:100797181-100797199 chr9:100797182-100797198 chr9:100797176-100797197 chr9:100797183-100797196
41	CTCF	chr9:100797100-100797250	GM12865	blood:	n/a	chr9:100797184-100797194 chr9:100797187-100797196 chr9:100797181-100797199 chr9:100797182-100797198 chr9:100797176-100797197 chr9:100797183-100797196
42	CTCF	chr9:100796989-100797398	GM12878	blood:	n/a	chr9:100797184-100797194 chr9:100797187-100797196 chr9:100797181-100797199 chr9:100797182-100797198 chr9:100797176-100797197 chr9:100797183-100797196
43	CTCF	chr9:100797960-100798110	HEK293	kidney:	n/a	n/a
44	CTCF	chr9:100797420-100797570	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr9:100801300-100801450	GM12867	blood:	n/a	n/a
46	CTCF	chr9:100797820-100797970	GM06990	blood:	n/a	n/a
47	CTCF	chr9:100797120-100797270	AG09309	skin:	n/a	chr9:100797184-100797194 chr9:100797187-100797196 chr9:100797181-100797199 chr9:100797182-100797198 chr9:100797176-100797197 chr9:100797183-100797196
48	CTCF	chr9:100797120-100797270	RPTEC	kidney:	n/a	chr9:100797184-100797194 chr9:100797187-100797196 chr9:100797181-100797199 chr9:100797182-100797198 chr9:100797176-100797197 chr9:100797183-100797196
49	CTCF	chr9:100801598-100801674	GM10266	blood:	n/a	n/a
50	CTCF	chr9:100797120-100797270	HPF	lung:	n/a	chr9:100797184-100797194 chr9:100797187-100797196 chr9:100797181-100797199 chr9:100797182-100797198 chr9:100797176-100797197 chr9:100797183-100797196

No.	Distal block	Cell Line	Cell type
1	chr9:100789228..100794108-chr9:100794751..100799924,8	K562	blood:
2	chr9:100684056..100686567-chr9:100797424..100799144,2	MCF-7	breast:
3	chr9:100744535..100746584-chr9:100805455..100807504,2	MCF-7	breast:
4	chr9:100744444..100747134-chr9:100785763..100788080,2	MCF-7	breast:
5	chr9:100781552..100783540-chr9:100791010..100793557,2	MCF-7	breast:
6	chr9:100799367..100802266-chr9:100805470..100807708,2	MCF-7	breast:
7	chr9:100744061..100747104-chr9:100795931..100798859,4	MCF-7	breast:
8	chr9:100788714..100791155-chr9:100817263..100819851,2	MCF-7	breast:
9	chr9:100684661..100686943-chr9:100794140..100799259,5	K562	blood:
10	chr9:100785373..100787194-chr9:100798359..100800018,2	K562	blood:
11	chr9:100743537..100749297-chr9:100805473..100813198,12	K562	blood:
12	chr9:100679327..100688755-chr9:100804829..100810921,12	K562	blood:
13	chr9:100803503..100806202-chr9:100818187..100820098,2	MCF-7	breast:
14	chr9:100796342..100798790-chr9:101837762..101839571,2	K562	blood:
15	chr9:100705623..100707205-chr9:100796922..100798794,2	K562	blood:
16	chr9:100776438..100779728-chr9:100795602..100798720,4	K562	blood:
17	chr9:100685785..100686517-chr9:100796418..100797247,3	MCF-7	breast:
18	chr9:100797145..100798657-chr9:100798784..100800862,2	K562	blood:
19	chr9:100746635..100749216-chr9:100789236..100791408,2	K562	blood:
20	chr9:100683608..100686455-chr9:100800996..100802948,2	K562	blood:
21	chr9:100685001..100687073-chr9:100804782..100806329,2	K562	blood:
22	chr9:100746098..100747887-chr9:100799710..100801330,2	K562	blood:
23	chr9:100767752..100769741-chr9:100788658..100791290,2	K562	blood:
24	chr9:100774780..100779950-chr9:100780337..100785356,9	K562	blood:
25	chr9:100683121..100685809-chr9:100788659..100790764,2	K562	blood:
26	chr9:100749336..100752167-chr9:100793207..100795151,3	K562	blood:
27	chr9:100799367..100802266-chr9:100805470..100807708,2	MCF-7	breast:
28	chr9:100785298..100787533-chr9:100792674..100795368,2	K562	blood:
29	chr9:100786498..100789736-chr9:100818544..100820292,3	MCF-7	breast:
30	chr9:100745634..100748414-chr9:100792592..100795011,2	MCF-7	breast:
31	chr9:100784033..100788653-chr9:100792674..100797277,7	K562	blood:
32	chr9:100685498..100686359-chr9:100796718..100798043,9	MCF-7	breast:
33	chr9:100769812..100771539-chr9:100787436..100790076,2	MCF-7	breast:
34	chr9:100796501..100799835-chr9:100807798..100809968,3	K562	blood:
35	chr9:100747352..100749216-chr9:100789908..100792300,2	K562	blood:
36	chr9:100789228..100794108-chr9:100794751..100799924,8	K562	blood:
37	chr9:100797529..100799265-chr9:100810758..100812808,2	K562	blood:
38	chr9:100785373..100787194-chr9:100798359..100800018,2	K562	blood:
39	chr9:100793900..100798932-chr9:100816820..100821233,8	MCF-7	breast:
40	chr9:100797667..100799438-chr9:100803367..100805131,2	MCF-7	breast:
41	chr9:100684268..100684829-chr9:100796846..100797760,2	K562	blood:
42	chr9:100685383..100686650-chr9:100796663..100797820,11	K562	blood:
43	chr9:100797145..100798657-chr9:100798784..100800862,2	K562	blood:
44	chr9:100779685..100780554-chr9:100797234..100797778,2	K562	blood:
45	chr9:100777690..100780620-chr9:100789410..100792089,2	MCF-7	breast:
46	chr9:100799859..100802210-chr9:100818612..100820734,3	K562	blood:
47	chr9:100797667..100799438-chr9:100803367..100805131,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANP32B-1	chr9:100788662-100789077	NONHSAT133544

Variant related genes	Relation type
RNU6-918P	TF binding region
ENSG00000136932	chromatin interactions
ENSG00000236896	chromatin interactions
ENSG00000136929	chromatin interactions
ENSG00000095380	chromatin interactions
ENSG00000212521	chromatin interactions
ENSG00000136938	chromatin interactions

Extended variants
information (count: 762 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549199074	chr9:100784653-100784654	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs12555343	chr9:100784659-100784660	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs185617392	chr9:100784661-100784662	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs551684001	chr9:100784669-100784670	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150007418	chr9:100784680-100784681	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs146557997	chr9:100784699-100784700	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs568984096	chr9:100784707-100784708	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs567418782	chr9:100784730-100784731	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544934400	chr9:100784753-100784754	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs536388336	chr9:100784754-100784755	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs556322155	chr9:100784764-100784765	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs202087722	chr9:100784781-100784782	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs368819727	chr9:100784792-100784793	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534760179	chr9:100784795-100784796	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs576256170	chr9:100784801-100784802	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs536407286	chr9:100784805-100784806	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs376210973	chr9:100784851-100784852	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188615956	chr9:100784867-100784868	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs116980805	chr9:100784875-100784876	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs150274181	chr9:100784900-100784901	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs181364361	chr9:100784913-100784914	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs367915934	chr9:100784976-100784977	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs540224397	chr9:100784980-100784981	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs141195003	chr9:100784998-100784999	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs573773689	chr9:100785017-100785018	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs116418496	chr9:100785076-100785077	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs558139352	chr9:100785105-100785106	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs562652887	chr9:100785130-100785131	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs531560439	chr9:100785162-100785163	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530386438	chr9:100785169-100785170	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs145582797	chr9:100785183-100785184	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs565195922	chr9:100785200-100785201	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369345466	chr9:100785209-100785210	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs547761122	chr9:100785242-100785243	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs138093090	chr9:100785267-100785268	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs149087442	chr9:100785319-100785320	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536323985	chr9:100785332-100785333	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs112628017	chr9:100785346-100785347	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs67308725	chr9:100785347-100785348	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs61686622	chr9:100785350-100785351	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs149021823	chr9:100785351-100785352	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs138086702	chr9:100785352-100785353	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs144861005	chr9:100785354-100785355	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142567423	chr9:100785355-100785356	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549882532	chr9:100785362-100785363	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs569879207	chr9:100785460-100785461	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs143108696	chr9:100785465-100785466	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs111706138	chr9:100785483-100785484	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs77407842	chr9:100785557-100785558	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs535050566	chr9:100785571-100785572	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD
Neurodevelopmental disorder	22521361	CNVD
Nicotine dependence	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100756600-100785600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
2	chr9:100757000-100785200	Strong transcription	Placenta	Placenta
3	chr9:100762600-100785400	Strong transcription	Primary T cells from cord blood	blood
4	chr9:100770600-100788400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:100773000-100784800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr9:100773200-100785600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
7	chr9:100776000-100785200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr9:100776400-100787400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr9:100778800-100788400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr9:100779000-100784800	Weak transcription	NH-A	brain
11	chr9:100780000-100785200	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr9:100780000-100788800	Weak transcription	Fetal Kidney	kidney
13	chr9:100781000-100785000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr9:100781200-100784800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:100781400-100788200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr9:100781800-100785800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr9:100781800-100786000	Weak transcription	Fetal Brain Female	brain
18	chr9:100781800-100788800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr9:100781800-100791800	Weak transcription	Hela-S3	cervix
20	chr9:100781800-100796800	Weak transcription	Brain Anterior Caudate	brain
21	chr9:100781800-100796800	Weak transcription	Colon Smooth Muscle	Colon
22	chr9:100782000-100787800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr9:100782000-100796800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr9:100782200-100784800	Weak transcription	Primary B cells from peripheral blood	blood
25	chr9:100782200-100785400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr9:100782200-100787400	Weak transcription	Brain Cingulate Gyrus	brain
27	chr9:100782200-100788000	Weak transcription	Colonic Mucosa	Colon
28	chr9:100782200-100788600	Weak transcription	K562	blood
29	chr9:100782200-100792400	Weak transcription	Aorta	Aorta
30	chr9:100782200-100794200	Weak transcription	NHDF-Ad	bronchial
31	chr9:100782200-100796800	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr9:100782200-100796800	Weak transcription	HepG2	liver
33	chr9:100782400-100785000	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr9:100782400-100785000	Weak transcription	Osteobl	bone
35	chr9:100782400-100787200	Weak transcription	Primary B cells from cord blood	blood
36	chr9:100782400-100796800	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr9:100782400-100797000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr9:100782800-100785000	Enhancers	Left Ventricle	heart
39	chr9:100782800-100785200	Enhancers	Right Ventricle	heart
40	chr9:100782800-100785800	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr9:100783000-100791200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr9:100783200-100785000	Strong transcription	Fetal Intestine Small	intestine
43	chr9:100783200-100785000	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr9:100783200-100785200	Strong transcription	Fetal Intestine Large	intestine
45	chr9:100783200-100786600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr9:100783400-100785400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr9:100783400-100785400	Enhancers	HUVEC	blood vessel
48	chr9:100783400-100786800	Weak transcription	HMEC	breast
49	chr9:100783600-100788400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr9:100783600-100789200	Weak transcription	Brain Germinal Matrix	brain

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