Variant report

Variant	nsv893477
Chromosome Location	chr9:78892526-78932928
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	chr9:78917903-78918226	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:78917918-78918291	K562	blood:	n/a	n/a
3	BHLHE40	chr9:78912579-78913109	K562	blood:	n/a	n/a
4	CEBPB	chr9:78915270-78915517	HepG2	liver:	n/a	chr9:78915383-78915394
5	CEBPB	chr9:78930471-78930559	A549	lung:	n/a	n/a
6	CEBPB	chr9:78931086-78931360	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr9:78930511-78930727	IMR90	lung:	n/a	n/a
8	CEBPB	chr9:78915338-78915527	K562	blood:	n/a	chr9:78915383-78915394
9	CEBPB	chr9:78930585-78930655	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr9:78905523-78905895	HepG2	liver:	n/a	n/a
11	CEBPB	chr9:78905560-78905800	A549	lung:	n/a	n/a
12	CEBPB	chr9:78905577-78905753	HepG2	liver:	n/a	n/a
13	CEBPB	chr9:78928227-78928322	HepG2	liver:	n/a	chr9:78928265-78928276
14	CEBPB	chr9:78905564-78905826	HepG2	liver:	n/a	n/a
15	CEBPB	chr9:78928294-78928301	A549	lung:	n/a	n/a
16	CTCF	chr9:78922100-78922250	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr9:78913716-78913953	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr9:78917853-78918202	K562	blood:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
19	CTCF	chr9:78922085-78922245	Fibrobl	skin:	n/a	n/a
20	CTCF	chr9:78917946-78918173	LNCaP	prostate:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
21	CTCF	chr9:78922088-78922258	MCF-7	breast:	n/a	n/a
22	CTCF	chr9:78917960-78918110	NHEK	skin:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
23	CTCF	chr9:78918000-78918150	NHDF-neo	bronchial:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
24	CTCF	chr9:78913700-78913850	HMEC	breast:	n/a	n/a
25	CTCF	chr9:78918080-78918230	WI-38	lung:	n/a	n/a
26	CTCF	chr9:78918060-78918210	HEK293	kidney:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
27	CTCF	chr9:78918000-78918150	HCT-116	colon:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
28	CTCF	chr9:78917939-78918206	Spleen_OC	spleen:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
29	CTCF	chr9:78917980-78918130	HEK293	kidney:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
30	CTCF	chr9:78918000-78918150	GM12872	blood:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
31	CTCF	chr9:78917843-78918281	A549	lung:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
32	CTCF	chr9:78918040-78918190	SAEC	small airway:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
33	CTCF	chr9:78917980-78918130	HPF	lung:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
34	CTCF	chr9:78918000-78918150	HMEC	breast:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
35	CTCF	chr9:78922100-78922250	RPTEC	kidney:	n/a	n/a
36	CTCF	chr9:78917980-78918130	AoAF	blood vessel:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
37	CTCF	chr9:78922100-78922250	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr9:78922100-78922250	HCT-116	colon:	n/a	n/a
39	CTCF	chr9:78918003-78918100	NHEK	skin:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
40	CTCF	chr9:78913760-78913910	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr9:78922140-78922290	HRE	kidney:	n/a	n/a
42	CTCF	chr9:78917980-78918130	HVMF	connective:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
43	CTCF	chr9:78913760-78913910	AG09319	gingival:	n/a	n/a
44	CTCF	chr9:78917960-78918110	HL-60	blood:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
45	CTCF	chr9:78922057-78922216	HepG2	liver:	n/a	n/a
46	CTCF	chr9:78917980-78918130	GM12878	blood:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
47	CTCF	chr9:78917960-78918110	HPF	lung:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
48	CTCF	chr9:78918180-78918330	A549	lung:	n/a	n/a
49	CTCF	chr9:78918000-78918150	GM12878	blood:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
50	CTCF	chr9:78913940-78914090	HFF	foreskin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:78912437-78912487	GM12891	blood:	n/a
2	chr9:78906644-78906694	GM12892	blood:	n/a
3	chr9:78905335-78905385	SK-N-SH	brain:	n/a
4	chr9:78906644-78906694	SAEC	small airway:	n/a
5	chr9:78905335-78905385	HepG2	liver:	n/a
6	chr9:78912437-78912487	IMR90	lung:	fetal
7	chr9:78905335-78905385	AG04449	skin:	fetal
8	chr9:78905335-78905385	NHBE	bronchial:	n/a
9	chr9:78905335-78905385	AG09309	skin:	n/a
10	chr9:78905335-78905385	SK-N-SH_RA	brain:	n/a
11	chr9:78905335-78905385	T-47D	breast:	n/a
12	chr9:78905335-78905385	HRCEpiC	kidney:	n/a
13	chr9:78906644-78906694	GM06990	blood:	n/a
14	chr9:78912437-78912487	HCF	heart:	n/a
15	chr9:78912437-78912487	HRPEpiC	eye:	n/a
16	chr9:78912437-78912487	HEEpiC	esophagus:	n/a
17	chr9:78906644-78906694	H1-hESC	embryonic stem cell:	embryo
18	chr9:78905335-78905385	GM12892	blood:	n/a
19	chr9:78906644-78906694	AoSMC	blood vessel:	n/a
20	chr9:78906644-78906694	AG10803	skin:	n/a
21	chr9:78906644-78906694	Jurkat	blood:	n/a
22	chr9:78912437-78912487	U87	brain:	n/a
23	chr9:78906644-78906694	ProgFib	skin:	n/a
24	chr9:78905335-78905385	Hepatocyte	liver:	n/a
25	chr9:78905335-78905385	HUVEC	blood vessel:	n/a
26	chr9:78912437-78912487	T-47D	breast:	n/a
27	chr9:78905335-78905385	Hela-S3	cervix:	n/a
28	chr9:78906644-78906694	GM12878	blood:	n/a
29	chr9:78905335-78905385	HCF	heart:	n/a
30	chr9:78912437-78912487	GM06990	blood:	n/a
31	chr9:78905335-78905385	ECC-1	luminal epithelium:	n/a
32	chr9:78906644-78906694	Hela-S3	cervix:	n/a
33	chr9:78905335-78905385	BJ	skin:	n/a
34	chr9:78912437-78912487	A549	lung:	n/a
35	chr9:78912437-78912487	K562	blood:	n/a
36	chr9:78912437-78912487	ECC-1	luminal epithelium:	n/a
37	chr9:78906644-78906694	Caco-2	colon:	n/a
38	chr9:78912437-78912487	SAEC	small airway:	n/a
39	chr9:78912437-78912487	MCF10A-Er-Src	breast:	n/a
40	chr9:78906644-78906694	K562	blood:	n/a
41	chr9:78905335-78905385	AG10803	skin:	n/a
42	chr9:78905335-78905385	GM12878	blood:	n/a
43	chr9:78905335-78905385	AG09319	gingival:	n/a
44	chr9:78905335-78905385	NT2-D1	testis:	n/a
45	chr9:78906644-78906694	HMEC	breast:	n/a
46	chr9:78905335-78905385	RPTEC	kidney:	n/a
47	chr9:78906644-78906694	PANC-1	pancreas:	n/a
48	chr9:78912437-78912487	HCM	heart:	n/a
49	chr9:78912437-78912487	AG04449	skin:	fetal
50	chr9:78906644-78906694	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:78701639..78702246-chr9:78917623..78918458,2	MCF-7	breast:
2	chr9:78917718..78920640-chr9:78922356..78925203,2	K562	blood:
3	chr9:78594386..78595229-chr9:78917510..78918589,3	MCF-7	breast:
4	chr9:78593987..78594566-chr9:78913006..78913887,2	MCF-7	breast:
5	chr9:78917718..78920640-chr9:78922356..78925203,2	K562	blood:
6	chr9:78593538..78594448-chr9:78917639..78918554,2	MCF-7	breast:
7	chr9:78624133..78625062-chr9:78913423..78914349,5	MCF-7	breast:
8	chr9:78834517..78835118-chr9:78917910..78918421,2	MCF-7	breast:
9	chr17:57918233..57920069-chr9:78928143..78930323,2	MCF-7	breast:

Variant related genes	Relation type
RBM22P5	TF binding region
RBM22P5	CpG island
ENSG00000199004	chromatin interactions

Extended variants
information (count: 1676 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1676 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3915861	chr9:78892526-78892527	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143997800	chr9:78892528-78892529	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113596615	chr9:78892558-78892559	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181862697	chr9:78892586-78892587	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569982652	chr9:78892639-78892640	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149689054	chr9:78892670-78892671	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545632845	chr9:78892712-78892713	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552451643	chr9:78892719-78892720	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565778378	chr9:78892732-78892733	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145376367	chr9:78892799-78892800	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531799290	chr9:78892843-78892844	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530760773	chr9:78892845-78892846	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75365408	chr9:78892858-78892859	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537379093	chr9:78892859-78892860	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12345311	chr9:78892863-78892864	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs577161484	chr9:78892871-78892872	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371270959	chr9:78892880-78892881	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545987829	chr9:78892894-78892895	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375755125	chr9:78893005-78893006	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12335946	chr9:78893013-78893014	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs7861583	chr9:78893058-78893059	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs573043142	chr9:78893075-78893076	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12345402	chr9:78893076-78893077	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs12345405	chr9:78893079-78893080	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs114618830	chr9:78893123-78893124	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369055838	chr9:78893166-78893167	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs77885146	chr9:78893167-78893168	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563644110	chr9:78893172-78893173	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145101968	chr9:78893217-78893218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77208049	chr9:78893227-78893228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552779912	chr9:78893255-78893256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373773315	chr9:78893343-78893344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566139524	chr9:78893384-78893385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146679430	chr9:78893413-78893414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147960303	chr9:78893453-78893454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10121296	chr9:78893476-78893477	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs187359923	chr9:78893536-78893537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs578095886	chr9:78893547-78893548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556955102	chr9:78893551-78893552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7851773	chr9:78893553-78893554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148874831	chr9:78893600-78893601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79200337	chr9:78893614-78893615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539347426	chr9:78893616-78893617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553157516	chr9:78893619-78893620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192130632	chr9:78893636-78893637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556749403	chr9:78893649-78893650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533578310	chr9:78893658-78893659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541972084	chr9:78893673-78893674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554666679	chr9:78893686-78893687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573413180	chr9:78893713-78893714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intellectual disability	22102821	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:78883000-78917200	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr9:78889600-78893200	Strong transcription	Fetal Intestine Small	intestine
3	chr9:78889800-78893400	Strong transcription	Fetal Intestine Large	intestine
4	chr9:78891400-78893200	Strong transcription	Duodenum Mucosa	Duodenum
5	chr9:78893200-78895400	Weak transcription	Fetal Intestine Small	intestine
6	chr9:78893200-78907200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr9:78893400-78900000	Weak transcription	Fetal Intestine Large	intestine
8	chr9:78893400-78910600	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr9:78895400-78895600	ZNF genes & repeats	Fetal Intestine Small	intestine
10	chr9:78895600-78901400	Weak transcription	Fetal Intestine Small	intestine
11	chr9:78900000-78900400	Strong transcription	Fetal Intestine Large	intestine
12	chr9:78900400-78901400	Weak transcription	Fetal Intestine Large	intestine
13	chr9:78901400-78901600	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr9:78901400-78903600	Strong transcription	Fetal Intestine Large	intestine
15	chr9:78901400-78904200	Strong transcription	Fetal Intestine Small	intestine
16	chr9:78901600-78902800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr9:78902200-78903200	Enhancers	Placenta	Placenta
18	chr9:78902400-78911800	Weak transcription	Small Intestine	intestine
19	chr9:78902800-78903200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr9:78903200-78904200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr9:78903200-78907400	Weak transcription	Placenta	Placenta
22	chr9:78903400-78917600	Weak transcription	Stomach Mucosa	stomach
23	chr9:78903600-78904800	Weak transcription	Fetal Intestine Large	intestine
24	chr9:78904200-78904400	Weak transcription	Fetal Intestine Small	intestine
25	chr9:78904200-78904600	Active TSS	Breast Myoepithelial Primary Cells	Breast
26	chr9:78904200-78904600	Enhancers	Fetal Brain Male	brain
27	chr9:78904200-78904600	Enhancers	Fetal Lung	lung
28	chr9:78904400-78905000	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr9:78904400-78905600	Enhancers	Fetal Intestine Small	intestine
30	chr9:78904600-78906200	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr9:78904600-78907400	Weak transcription	Fetal Lung	lung
32	chr9:78904600-78911400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr9:78904800-78905400	Enhancers	Fetal Intestine Large	intestine
34	chr9:78905000-78907400	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr9:78905200-78905800	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr9:78905200-78905800	Enhancers	Fetal Muscle Leg	muscle
37	chr9:78905200-78905800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr9:78905200-78905800	Enhancers	HepG2	liver
39	chr9:78905400-78906000	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr9:78905400-78906000	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr9:78905400-78906600	Weak transcription	Fetal Intestine Large	intestine
42	chr9:78905600-78907200	Weak transcription	Fetal Intestine Small	intestine
43	chr9:78905800-78907200	Weak transcription	Fetal Muscle Leg	muscle
44	chr9:78905800-78922400	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr9:78906000-78912800	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr9:78906200-78907000	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr9:78906600-78911600	Strong transcription	Fetal Intestine Large	intestine
48	chr9:78907000-78907200	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr9:78907000-78907600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr9:78907200-78907400	Enhancers	Adipose Nuclei	Adipose

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