Variant report

Variant	nsv893418
Chromosome Location	chr9:71624695-71633767
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:63)
CpG islands
(count:305)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:63 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71631852-71631872	K562	blood:	n/a	n/a
2	BHLHE40	chr9:71631696-71631742	K562	blood:	n/a	n/a
3	BHLHE40	chr9:71633440-71634093	K562	blood:	n/a	n/a
4	CTCF	chr9:71627811-71627880	GM19239	blood:	n/a	n/a
5	CTCF	chr9:71627799-71627948	GM12892	blood:	n/a	n/a
6	CTCF	chr9:71633740-71633890	GM12872	blood:	n/a	n/a
7	CTCF	chr9:71633740-71633890	GM12875	blood:	n/a	n/a
8	CTCF	chr9:71633660-71633810	GM12865	blood:	n/a	n/a
9	CTCF	chr9:71628340-71628490	GM12873	blood:	n/a	n/a
10	CTCF	chr9:71633720-71633870	GM06990	blood:	n/a	n/a
11	CTCF	chr9:71627804-71627970	GM19240	blood:	n/a	n/a
12	CTCF	chr9:71629112-71629136	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr9:71628173-71628180	GM13976	blood:	n/a	n/a
14	CTCF	chr9:71633760-71633910	GM12872	blood:	n/a	n/a
15	CTCF	chr9:71629142-71629173	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr9:71627840-71627990	GM12871	blood:	n/a	n/a
17	CTCF	chr9:71633670-71633989	K562	blood:	n/a	n/a
18	CTCF	chr9:71633760-71633910	GM12864	blood:	n/a	n/a
19	CTCF	chr9:71633749-71633908	K562	blood:	n/a	n/a
20	CTCF	chr9:71633675-71633960	GM12878	blood:	n/a	n/a
21	CTCF	chr9:71633748-71633899	GM12878	blood:	n/a	n/a
22	CTCF	chr9:71627821-71627937	GM19238	blood:	n/a	n/a
23	CTCF	chr9:71633760-71633910	GM12865	blood:	n/a	n/a
24	CTCF	chr9:71633720-71633870	GM12868	blood:	n/a	n/a
25	CTCF	chr9:71628120-71628170	GM13976	blood:	n/a	n/a
26	CTCF	chr9:71633760-71633910	GM12873	blood:	n/a	n/a
27	CTCF	chr9:71627900-71628050	GM12873	blood:	n/a	n/a
28	FOS	chr9:71624718-71624895	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr9:71624669-71624951	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr9:71624680-71624859	MCF10A-Er-Src	breast:	n/a	n/a
31	GATA1	chr9:71633155-71634255	PBDE	blood:	n/a	n/a
32	MAX	chr9:71633696-71633853	NB4	blood:	n/a	chr9:71633752-71633762 chr9:71633756-71633772
33	MAX	chr9:71633610-71633932	K562	blood:	n/a	chr9:71633752-71633762 chr9:71633756-71633772
34	MAX	chr9:71633526-71633959	K562	blood:	n/a	chr9:71633752-71633762 chr9:71633756-71633772
35	MYC	chr9:71624786-71624827	MCF10A-Er-Src	breast:	n/a	n/a
36	MYC	chr9:71633601-71633987	K562	blood:	n/a	chr9:71633752-71633762 chr9:71633756-71633772
37	MYC	chr9:71631770-71631867	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr9:71628579-71628772	MCF-7	breast:	n/a	n/a
39	POLR2A	chr9:71628632-71628766	MCF-7	breast:	n/a	n/a
40	POLR2A	chr9:71627881-71628420	HL-60	blood:	n/a	n/a
41	POLR2A	chr9:71628412-71628574	Gliobla	brain:	n/a	n/a
42	POLR2A	chr9:71630581-71630643	GM12878	blood:	n/a	n/a
43	POLR2A	chr9:71627887-71628340	HL-60	blood:	n/a	n/a
44	POLR2A	chr9:71630658-71630663	GM12878	blood:	n/a	n/a
45	POLR2A	chr9:71631484-71631528	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr9:71628639-71628655	Gliobla	brain:	n/a	n/a
47	POLR2A	chr9:71628595-71628611	Gliobla	brain:	n/a	n/a
48	RAD21	chr9:71633607-71634011	HepG2	liver:	n/a	n/a
49	RAD21	chr9:71633656-71633895	GM12878	blood:	n/a	n/a
50	RAD21	chr9:71633713-71633879	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71627667-71627717	GM12878	blood:	n/a
2	chr9:71627524-71627574	HIPEpiC	eye:	n/a
3	chr9:71628906-71628956	NHDF-neo	bronchial:	n/a
4	chr9:71627667-71627717	BJ	skin:	n/a
5	chr9:71628906-71628956	GM12892	blood:	n/a
6	chr9:71627667-71627717	PANC-1	pancreas:	n/a
7	chr9:71631514-71631564	HUVEC	blood vessel:	n/a
8	chr9:71629130-71629180	GM12891	blood:	n/a
9	chr9:71631514-71631564	HCT-116	colon:	n/a
10	chr9:71631514-71631564	T-47D	breast:	n/a
11	chr9:71629130-71629180	RPTEC	kidney:	n/a
12	chr9:71628906-71628956	Hepatocyte	liver:	n/a
13	chr9:71628906-71628956	ProgFib	skin:	n/a
14	chr9:71627667-71627717	HUVEC	blood vessel:	n/a
15	chr9:71629130-71629180	NHBE	bronchial:	n/a
16	chr9:71629130-71629180	BE2_C	brain:	n/a
17	chr9:71631514-71631564	A549	lung:	n/a
18	chr9:71627667-71627717	GM12891	blood:	n/a
19	chr9:71627667-71627717	GM19239	blood:	n/a
20	chr9:71631514-71631564	K562	blood:	n/a
21	chr9:71627524-71627574	CMK	blood:	n/a
22	chr9:71627667-71627717	H1-hESC	embryonic stem cell:	embryo
23	chr9:71629130-71629180	HepG2	liver:	n/a
24	chr9:71631514-71631564	GM12891	blood:	n/a
25	chr9:71629130-71629180	BJ	skin:	n/a
26	chr9:71631514-71631564	MCF10A-Er-Src	breast:	n/a
27	chr9:71631514-71631564	HEEpiC	esophagus:	n/a
28	chr9:71631514-71631564	HRE	kidney:	n/a
29	chr9:71627524-71627574	A549	lung:	n/a
30	chr9:71627524-71627574	HCM	heart:	n/a
31	chr9:71631514-71631564	AG09309	skin:	n/a
32	chr9:71628906-71628956	SKMC	muscle:	n/a
33	chr9:71627524-71627574	AG09319	gingival:	n/a
34	chr9:71629130-71629180	HL-60	blood:	n/a
35	chr9:71627667-71627717	ProgFib	skin:	n/a
36	chr9:71628906-71628956	HCF	heart:	n/a
37	chr9:71627667-71627717	AG09309	skin:	n/a
38	chr9:71627524-71627574	HRPEpiC	eye:	n/a
39	chr9:71627524-71627574	HepG2	liver:	n/a
40	chr9:71627667-71627717	HL-60	blood:	n/a
41	chr9:71628906-71628956	NT2-D1	testis:	n/a
42	chr9:71627524-71627574	BE2_C	brain:	n/a
43	chr9:71628906-71628956	HL-60	blood:	n/a
44	chr9:71631514-71631564	NH-A	brain:	n/a
45	chr9:71631514-71631564	IMR90	lung:	fetal
46	chr9:71628906-71628956	CMK	blood:	n/a
47	chr9:71627667-71627717	RPTEC	kidney:	n/a
48	chr9:71627524-71627574	SK-N-SH	brain:	n/a
49	chr9:71629130-71629180	PANC-1	pancreas:	n/a
50	chr9:71629130-71629180	GM12878	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:71622551..71625318-chr9:71628981..71631159,4	K562	blood:
2	chr9:71621939..71625091-chr9:71631557..71634181,3	K562	blood:
3	chr9:71627843..71630592-chr9:71632071..71633725,3	K562	blood:
4	chr9:71621939..71625091-chr9:71631557..71634181,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKACG-4	chr9:71624143-71625000	ucscGeneNc_uc004ahk_2
2	lnc-PRKACG-4	chr9:71625289-71625403	ucscGeneNc_uc004ahk_2

No data

Variant related genes	Relation type
PRKACG	TF binding region
PRKACG	CpG island
ENSG00000165059	chromatin interactions

Extended variants
information (count: 373 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs872077	chr9:71624695-71624696	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs116807043	chr9:71624714-71624715	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs575303064	chr9:71624720-71624721	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs142291409	chr9:71624743-71624744	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs200923844	chr9:71624746-71624747	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs542127693	chr9:71624799-71624800	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs550153882	chr9:71624834-71624835	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs147867683	chr9:71624842-71624843	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs141883689	chr9:71624873-71624874	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs74647651	chr9:71624920-71624921	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs34498152	chr9:71624942-71624943	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs566667216	chr9:71624970-71624971	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs147102301	chr9:71624974-71624975	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs555300439	chr9:71625005-71625006	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574970777	chr9:71625102-71625103	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535994830	chr9:71625132-71625133	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs188569397	chr9:71625183-71625184	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs35451405	chr9:71625194-71625195	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs74493939	chr9:71625195-71625196	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs397758254	chr9:71625204-71625205	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs376610609	chr9:71625237-71625238	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs141066694	chr9:71625256-71625257	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532223470	chr9:71625268-71625269	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs371688707	chr9:71625289-71625290	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs150245139	chr9:71625310-71625311	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs138544007	chr9:71625353-71625354	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs573483752	chr9:71625354-71625355	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs574809838	chr9:71625393-71625394	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs112083034	chr9:71625406-71625407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565489755	chr9:71625407-71625408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561982152	chr9:71625433-71625434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528389757	chr9:71625434-71625435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548043870	chr9:71625445-71625446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs5898054	chr9:71625450-71625451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs41296858	chr9:71625510-71625511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs202083597	chr9:71625527-71625528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375918651	chr9:71625537-71625538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11324045	chr9:71625550-71625551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs3067086	chr9:71625570-71625571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568325648	chr9:71625584-71625585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528950256	chr9:71625592-71625593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537099456	chr9:71625608-71625609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567305104	chr9:71625670-71625671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532909516	chr9:71625677-71625678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76572035	chr9:71625714-71625715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs180751627	chr9:71625721-71625722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79664078	chr9:71625727-71625728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs41296856	chr9:71625728-71625729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184528199	chr9:71625735-71625736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549190880	chr9:71625743-71625744	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
Melanoma	22183965	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
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	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
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71594800-71628400	Weak transcription	Spleen	Spleen
2	chr9:71595200-71628000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:71595200-71631600	Weak transcription	Gastric	stomach
4	chr9:71595800-71626200	Weak transcription	Colonic Mucosa	Colon
5	chr9:71597200-71626000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr9:71598800-71644600	Weak transcription	Right Atrium	heart
7	chr9:71606800-71626800	Weak transcription	HepG2	liver
8	chr9:71607400-71630600	Weak transcription	Aorta	Aorta
9	chr9:71607600-71628000	Weak transcription	Lung	lung
10	chr9:71614600-71625200	Weak transcription	Fetal Stomach	stomach
11	chr9:71614600-71625800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr9:71614600-71626800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr9:71614600-71626800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr9:71614600-71627400	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr9:71614600-71630800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:71614800-71627400	Weak transcription	GM12878-XiMat	blood
17	chr9:71618200-71625000	Strong transcription	Fetal Intestine Large	intestine
18	chr9:71619000-71631200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr9:71619600-71627800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr9:71619600-71631600	Weak transcription	Left Ventricle	heart
21	chr9:71620800-71625000	Strong transcription	Rectal Mucosa Donor 29	rectum
22	chr9:71621000-71625400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr9:71621200-71625000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr9:71621400-71624800	Strong transcription	Primary B cells from cord blood	blood
25	chr9:71622200-71634600	Weak transcription	Fetal Heart	heart
26	chr9:71623000-71625000	Strong transcription	Duodenum Mucosa	Duodenum
27	chr9:71623400-71631600	Weak transcription	Pancreas	Pancrea
28	chr9:71624000-71627000	Weak transcription	Primary B cells from peripheral blood	blood
29	chr9:71624400-71625200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr9:71624400-71625200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr9:71624400-71625400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr9:71624400-71625400	Enhancers	NHEK	skin
33	chr9:71624600-71626200	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr9:71624600-71628000	Weak transcription	Fetal Intestine Small	intestine
35	chr9:71624600-71630600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr9:71624800-71627000	Weak transcription	Primary B cells from cord blood	blood
37	chr9:71625000-71626800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr9:71625000-71628000	Weak transcription	Fetal Intestine Large	intestine
39	chr9:71625000-71628200	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr9:71625000-71634600	Weak transcription	Duodenum Mucosa	Duodenum
41	chr9:71625400-71628000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:71626800-71627000	Enhancers	HepG2	liver
43	chr9:71626800-71627400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr9:71626800-71627600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr9:71626800-71627600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr9:71626800-71628400	Enhancers	Primary hematopoietic stem cells	blood
47	chr9:71627000-71627800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr9:71627000-71627800	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr9:71627000-71628000	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr9:71627000-71628400	Enhancers	Primary B cells from cord blood	blood

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