Variant report

Variant	nsv893417
Chromosome Location	chr9:71621687-71633767
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:74)
CpG islands
(count:366)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:74 , 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	chr9:71633440-71634093	K562	blood:	n/a	n/a
3	BHLHE40	chr9:71631696-71631742	K562	blood:	n/a	n/a
4	CCNT2	chr9:71623403-71623461	K562	blood:	n/a	n/a
5	CEBPB	chr9:71622410-71622544	K562	blood:	n/a	chr9:71622451-71622462
6	CEBPB	chr9:71622329-71622529	HepG2	liver:	n/a	chr9:71622451-71622462
7	CEBPB	chr9:71622344-71622530	IMR90	lung:	n/a	chr9:71622451-71622462
8	CTCF	chr9:71633760-71633910	GM12873	blood:	n/a	n/a
9	CTCF	chr9:71633740-71633890	GM12872	blood:	n/a	n/a
10	CTCF	chr9:71629112-71629136	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr9:71627811-71627880	GM19239	blood:	n/a	n/a
12	CTCF	chr9:71627821-71627937	GM19238	blood:	n/a	n/a
13	CTCF	chr9:71633720-71633870	GM06990	blood:	n/a	n/a
14	CTCF	chr9:71629142-71629173	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr9:71633740-71633890	GM12875	blood:	n/a	n/a
16	CTCF	chr9:71633748-71633899	GM12878	blood:	n/a	n/a
17	CTCF	chr9:71633720-71633870	GM12868	blood:	n/a	n/a
18	CTCF	chr9:71633760-71633910	GM12865	blood:	n/a	n/a
19	CTCF	chr9:71628120-71628170	GM13976	blood:	n/a	n/a
20	CTCF	chr9:71627900-71628050	GM12873	blood:	n/a	n/a
21	CTCF	chr9:71628340-71628490	GM12873	blood:	n/a	n/a
22	CTCF	chr9:71627804-71627970	GM19240	blood:	n/a	n/a
23	CTCF	chr9:71633675-71633960	GM12878	blood:	n/a	n/a
24	CTCF	chr9:71627799-71627948	GM12892	blood:	n/a	n/a
25	CTCF	chr9:71633760-71633910	GM12872	blood:	n/a	n/a
26	CTCF	chr9:71633760-71633910	GM12864	blood:	n/a	n/a
27	CTCF	chr9:71627840-71627990	GM12871	blood:	n/a	n/a
28	CTCF	chr9:71633749-71633908	K562	blood:	n/a	n/a
29	CTCF	chr9:71628173-71628180	GM13976	blood:	n/a	n/a
30	CTCF	chr9:71633660-71633810	GM12865	blood:	n/a	n/a
31	CTCF	chr9:71633670-71633989	K562	blood:	n/a	n/a
32	FOS	chr9:71624680-71624859	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr9:71624718-71624895	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr9:71624669-71624951	MCF10A-Er-Src	breast:	n/a	n/a
35	GATA1	chr9:71633155-71634255	PBDE	blood:	n/a	n/a
36	MAX	chr9:71633696-71633853	NB4	blood:	n/a	chr9:71633752-71633762 chr9:71633756-71633772
37	MAX	chr9:71633526-71633959	K562	blood:	n/a	chr9:71633752-71633762 chr9:71633756-71633772
38	MAX	chr9:71633610-71633932	K562	blood:	n/a	chr9:71633752-71633762 chr9:71633756-71633772
39	MYC	chr9:71633601-71633987	K562	blood:	n/a	chr9:71633752-71633762 chr9:71633756-71633772
40	MYC	chr9:71623181-71623226	MCF10A-Er-Src	breast:	n/a	n/a
41	MYC	chr9:71624786-71624827	MCF10A-Er-Src	breast:	n/a	n/a
42	MYC	chr9:71631770-71631867	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr9:71628412-71628574	Gliobla	brain:	n/a	n/a
44	POLR2A	chr9:71628639-71628655	Gliobla	brain:	n/a	n/a
45	POLR2A	chr9:71631484-71631528	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr9:71623211-71623237	HepG2	liver:	n/a	n/a
47	POLR2A	chr9:71623414-71623452	HepG2	liver:	n/a	n/a
48	POLR2A	chr9:71628595-71628611	Gliobla	brain:	n/a	n/a
49	POLR2A	chr9:71630658-71630663	GM12878	blood:	n/a	n/a
50	POLR2A	chr9:71627881-71628420	HL-60	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71629130-71629180	A549	lung:	n/a
2	chr9:71631514-71631564	HCF	heart:	n/a
3	chr9:71623401-71623451	AG04449	skin:	fetal
4	chr9:71627667-71627717	HPAEpiC	pulmonary alveolar:	n/a
5	chr9:71631514-71631564	HEEpiC	esophagus:	n/a
6	chr9:71627524-71627574	HL-60	blood:	n/a
7	chr9:71628906-71628956	Hela-S3	cervix:	n/a
8	chr9:71627667-71627717	Jurkat	blood:	n/a
9	chr9:71627524-71627574	PANC-1	pancreas:	n/a
10	chr9:71629130-71629180	HPAEpiC	pulmonary alveolar:	n/a
11	chr9:71627524-71627574	AG09319	gingival:	n/a
12	chr9:71627524-71627574	AG04450	lung:	fetal
13	chr9:71631514-71631564	HNPCEpiC	eye:	n/a
14	chr9:71623401-71623451	HL-60	blood:	n/a
15	chr9:71627667-71627717	NHDF-neo	bronchial:	n/a
16	chr9:71629130-71629180	NHBE	bronchial:	n/a
17	chr9:71628906-71628956	GM06990	blood:	n/a
18	chr9:71627667-71627717	AG09309	skin:	n/a
19	chr9:71628906-71628956	HRE	kidney:	n/a
20	chr9:71631514-71631564	AG09309	skin:	n/a
21	chr9:71629130-71629180	HEK293	kidney:	embryo
22	chr9:71627667-71627717	NHBE	bronchial:	n/a
23	chr9:71629130-71629180	SKMC	muscle:	n/a
24	chr9:71629130-71629180	ovcar-3	ovarian:	n/a
25	chr9:71623401-71623451	ProgFib	skin:	n/a
26	chr9:71627524-71627574	HCPEpiC	choroid plexus:	n/a
27	chr9:71631514-71631564	HepG2	liver:	n/a
28	chr9:71631514-71631564	HEK293	kidney:	embryo
29	chr9:71628906-71628956	NB4	blood:	n/a
30	chr9:71631514-71631564	IMR90	lung:	fetal
31	chr9:71623401-71623451	T-47D	breast:	n/a
32	chr9:71627667-71627717	GM06990	blood:	n/a
33	chr9:71629130-71629180	AG04449	skin:	fetal
34	chr9:71623401-71623451	BJ	skin:	n/a
35	chr9:71631514-71631564	Hela-S3	cervix:	n/a
36	chr9:71623401-71623451	HEK293	kidney:	embryo
37	chr9:71629130-71629180	HRCEpiC	kidney:	n/a
38	chr9:71631514-71631564	NB4	blood:	n/a
39	chr9:71623401-71623451	K562	blood:	n/a
40	chr9:71631514-71631564	MCF10A-Er-Src	breast:	n/a
41	chr9:71627524-71627574	HepG2	liver:	n/a
42	chr9:71628906-71628956	LNCaP	prostate:	n/a
43	chr9:71627667-71627717	SAEC	small airway:	n/a
44	chr9:71629130-71629180	T-47D	breast:	n/a
45	chr9:71627524-71627574	IMR90	lung:	fetal
46	chr9:71627667-71627717	SKMC	muscle:	n/a
47	chr9:71627667-71627717	CMK	blood:	n/a
48	chr9:71628906-71628956	ovcar-3	ovarian:	n/a
49	chr9:71629130-71629180	Hela-S3	cervix:	n/a
50	chr9:71631514-71631564	HUVEC	blood vessel:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 508 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10869690	chr9:71621687-71621688	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537812775	chr9:71621704-71621705	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556166869	chr9:71621786-71621787	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs367865297	chr9:71621802-71621803	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547380841	chr9:71621845-71621846	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79442670	chr9:71621867-71621868	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs111269867	chr9:71621870-71621871	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189074946	chr9:71621875-71621876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536522059	chr9:71621900-71621901	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140913185	chr9:71621911-71621912	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1541083	chr9:71621922-71621923	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs549952875	chr9:71621939-71621940	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556902162	chr9:71621951-71621952	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376529846	chr9:71621956-71621957	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150190611	chr9:71621965-71621966	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139397523	chr9:71621979-71621980	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570219683	chr9:71621988-71621989	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564905719	chr9:71621995-71621996	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181117984	chr9:71622017-71622018	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373380090	chr9:71622053-71622054	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1541082	chr9:71622100-71622101	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs559601012	chr9:71622136-71622137	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78014488	chr9:71622226-71622227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548379843	chr9:71622257-71622258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141842817	chr9:71622266-71622267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72722073	chr9:71622288-71622289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369035062	chr9:71622318-71622319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185664759	chr9:71622336-71622337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188126176	chr9:71622395-71622396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4745497	chr9:71622484-71622485	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs180954551	chr9:71622495-71622496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187001800	chr9:71622499-71622500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11144747	chr9:71622501-71622502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555232606	chr9:71622502-71622503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192374674	chr9:71622506-71622507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537181463	chr9:71622509-71622510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147092280	chr9:71622511-71622512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181514483	chr9:71622512-71622513	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541029344	chr9:71622539-71622540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559349449	chr9:71622540-71622541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138455631	chr9:71622544-71622545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186026446	chr9:71622548-71622549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190741114	chr9:71622556-71622557	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs368563242	chr9:71622559-71622560	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs386734754	chr9:71622567-71622568	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs565049182	chr9:71622569-71622570	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs546359232	chr9:71622570-71622571	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs547795305	chr9:71622574-71622575	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs566223274	chr9:71622580-71622581	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547562582	chr9:71622581-71622582	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	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:184 , 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	chr9:71598800-71623200	Weak transcription	Pancreas	Pancrea
7	chr9:71598800-71644600	Weak transcription	Right Atrium	heart
8	chr9:71606800-71623000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr9:71606800-71626800	Weak transcription	HepG2	liver
10	chr9:71607400-71630600	Weak transcription	Aorta	Aorta
11	chr9:71607600-71628000	Weak transcription	Lung	lung
12	chr9:71613000-71624600	Strong transcription	Fetal Intestine Small	intestine
13	chr9:71614600-71623000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:71614600-71625200	Weak transcription	Fetal Stomach	stomach
15	chr9:71614600-71625800	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr9:71614600-71626800	Weak transcription	Primary hematopoietic stem cells	blood
17	chr9:71614600-71626800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:71614600-71627400	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr9:71614600-71630800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:71614800-71627400	Weak transcription	GM12878-XiMat	blood
21	chr9:71618200-71625000	Strong transcription	Fetal Intestine Large	intestine
22	chr9:71619000-71631200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr9:71619600-71623600	Weak transcription	Rectal Smooth Muscle	rectum
24	chr9:71619600-71627800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr9:71619600-71631600	Weak transcription	Left Ventricle	heart
26	chr9:71620000-71623000	Weak transcription	Primary B cells from peripheral blood	blood
27	chr9:71620000-71623000	Weak transcription	Right Ventricle	heart
28	chr9:71620800-71625000	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr9:71621000-71625400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr9:71621200-71622200	Strong transcription	Duodenum Mucosa	Duodenum
31	chr9:71621200-71625000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr9:71621400-71622200	Enhancers	Fetal Heart	heart
33	chr9:71621400-71624800	Strong transcription	Primary B cells from cord blood	blood
34	chr9:71622200-71623000	Weak transcription	Duodenum Mucosa	Duodenum
35	chr9:71622200-71634600	Weak transcription	Fetal Heart	heart
36	chr9:71623000-71623200	Enhancers	Ovary	ovary
37	chr9:71623000-71623200	Enhancers	Right Ventricle	heart
38	chr9:71623000-71623800	Enhancers	Fetal Brain Male	brain
39	chr9:71623000-71624000	Strong transcription	Primary B cells from peripheral blood	blood
40	chr9:71623000-71624600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr9:71623000-71624600	Strong transcription	Rectal Mucosa Donor 31	rectum
42	chr9:71623000-71625000	Strong transcription	Duodenum Mucosa	Duodenum
43	chr9:71623200-71623400	ZNF genes & repeats	Pancreas	Pancrea
44	chr9:71623400-71631600	Weak transcription	Pancreas	Pancrea
45	chr9:71624000-71627000	Weak transcription	Primary B cells from peripheral blood	blood
46	chr9:71624400-71625200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr9:71624400-71625200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr9:71624400-71625400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr9:71624400-71625400	Enhancers	NHEK	skin
50	chr9:71624600-71626200	Weak transcription	Rectal Mucosa Donor 31	rectum

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