Variant report

Variant	nsv466511
Chromosome Location	chr9:116374990-116397397
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:568)
CpG islands
(count:0)
Chromatin interactive
region (count:34)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:568 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:116384914-116385574	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:116382820-116383077	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:116376294-116376349	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:116391132-116391133	HepG2	liver:	n/a	n/a
5	ATF2	chr9:116382718-116383223	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:116385186-116385785	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:116385103-116385621	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr9:116382711-116383313	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr9:116382699-116383222	A549	lung:	n/a	n/a
10	ATF3	chr9:116382824-116383173	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr9:116382768-116383032	K562	blood:	n/a	n/a
12	BACH1	chr9:116385319-116385849	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr9:116396127-116396646	HepG2	liver:	n/a	n/a
14	BHLHE40	chr9:116396332-116396620	K562	blood:	n/a	n/a
15	BHLHE40	chr9:116377619-116377877	GM12878	blood:	n/a	n/a
16	CCNT2	chr9:116375263-116375436	K562	blood:	n/a	n/a
17	CEBPB	chr9:116382792-116383041	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr9:116394328-116394654	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:116394946-116395391	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:116377193-116377726	IMR90	lung:	n/a	n/a
21	CEBPB	chr9:116382888-116383139	HepG2	liver:	n/a	n/a
22	CEBPB	chr9:116382813-116383073	IMR90	lung:	n/a	n/a
23	CEBPB	chr9:116385265-116385559	IMR90	lung:	n/a	n/a
24	CEBPB	chr9:116385185-116385485	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr9:116382840-116383098	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr9:116382889-116383066	HepG2	liver:	n/a	n/a
27	CHD2	chr9:116377356-116377805	GM12878	blood:	n/a	n/a
28	CHD2	chr9:116382786-116383006	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr9:116385498-116385611	HepG2	liver:	n/a	n/a
30	CHD2	chr9:116385248-116385621	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr9:116382848-116383196	Hela-S3	cervix:	n/a	n/a
32	CREB1	chr9:116385163-116385556	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr9:116376240-116376390	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr9:116379234-116379273	GM12891	blood:	n/a	n/a
35	CTCF	chr9:116383300-116383450	HAc	cerebellar:	n/a	n/a
36	CTCF	chr9:116384021-116384087	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr9:116379140-116379290	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr9:116383760-116383910	AG10803	skin:	n/a	n/a
39	CTCF	chr9:116379060-116379210	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr9:116383800-116383950	AG04449	skin:	n/a	n/a
41	CTCF	chr9:116379183-116379375	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr9:116389320-116389470	GM12874	blood:	n/a	n/a
43	CTCF	chr9:116383780-116383930	NHDF-neo	bronchial:	n/a	n/a
44	CUX1	chr9:116384973-116385532	GM12878	blood:	n/a	chr9:116384994-116385005
45	CUX1	chr9:116377406-116377580	GM12878	blood:	n/a	chr9:116377536-116377545
46	E2F4	chr9:116382865-116383085	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F6	chr9:116382587-116383201	A549	lung:	n/a	n/a
48	E2F6	chr9:116378958-116379531	H1-hESC	embryonic stem cell:	n/a	n/a
49	E2F6	chr9:116382678-116383037	H1-hESC	embryonic stem cell:	n/a	n/a
50	E2F6	chr9:116382533-116383200	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:116383635..116386801-chr9:116393462..116397071,5	MCF-7	breast:
2	chr9:116376834..116379828-chr9:116381468..116382973,2	MCF-7	breast:
3	chr9:116388280..116391769-chr9:116395247..116396966,3	MCF-7	breast:
4	chr9:116393296..116396126-chr9:116417264..116418987,2	MCF-7	breast:
5	chr9:116376628..116378313-chr9:116382222..116384609,3	MCF-7	breast:
6	chr9:116368318..116370482-chr9:116376784..116379532,2	MCF-7	breast:
7	chr9:116382976..116384778-chr9:116398456..116400066,2	MCF-7	breast:
8	chr9:116382263..116386126-chr9:116386783..116389124,3	MCF-7	breast:
9	chr9:116383635..116386801-chr9:116393462..116397071,5	MCF-7	breast:
10	chr9:116368954..116370603-chr9:116373905..116376244,2	MCF-7	breast:
11	chr9:116392305..116395161-chr9:116397306..116400059,2	MCF-7	breast:
12	chr9:116172702..116174409-chr9:116381360..116383255,2	MCF-7	breast:
13	chr9:116383167..116386391-chr9:116389906..116398638,8	MCF-7	breast:
14	chr9:116376628..116378313-chr9:116382222..116384609,3	MCF-7	breast:
15	chr9:116378512..116381632-chr9:116384610..116387755,3	MCF-7	breast:
16	chr9:116388280..116391769-chr9:116395247..116396966,3	MCF-7	breast:
17	chr9:116384013..116386920-chr9:116410896..116413460,2	MCF-7	breast:
18	chr9:116364314..116366664-chr9:116377313..116378930,2	MCF-7	breast:
19	chr9:116396277..116398394-chr9:116409096..116411903,2	MCF-7	breast:
20	chr9:116356309..116357937-chr9:116375558..116377978,2	MCF-7	breast:
21	chr9:116371231..116372845-chr9:116374624..116376242,2	MCF-7	breast:
22	chr9:116362421..116364215-chr9:116382528..116385259,2	MCF-7	breast:
23	chr9:116385601..116388209-chr9:116407553..116409087,2	MCF-7	breast:
24	chr9:116385537..116387562-chr9:116409870..116412944,3	MCF-7	breast:
25	chr9:116373324..116375940-chr9:116380563..116382794,2	MCF-7	breast:
26	chr9:116386561..116388140-chr9:116399851..116401503,2	MCF-7	breast:
27	chr9:116395680..116398027-chr9:116408814..116410400,2	MCF-7	breast:
28	chr9:116382263..116386126-chr9:116386783..116389124,3	MCF-7	breast:
29	chr9:116375318..116378265-chr9:116400477..116402122,2	K562	blood:
30	chr9:116383167..116386391-chr9:116389906..116398638,8	MCF-7	breast:
31	chr9:116387727..116389592-chr9:116393862..116395666,2	K562	blood:
32	chr9:116379738..116382118-chr9:116392822..116396167,3	MCF-7	breast:
33	chr9:116387727..116389592-chr9:116393862..116395666,2	K562	blood:
34	chr9:116392305..116395161-chr9:116397306..116400059,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS3-1	chr9:116381508-116381691	ENSG00000233817
2	lnc-RGS3-1	chr9:116382056-116384914	ENSG00000233817

No data

Variant related genes	Relation type
ENSG00000233817	TF binding region
ENSG00000227482	chromatin interactions
ENSG00000148229	chromatin interactions
ENSG00000233817	chromatin interactions
ENSG00000157653	chromatin interactions
ENSG00000138835	chromatin interactions
SIPA1L2	miRNA target sites
LPHN1	miRNA target sites

Extended variants
information (count: 889 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:889 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs591426	chr9:116374990-116374991	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370398262	chr9:116374991-116374992	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs785099	chr9:116375013-116375014	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs785100	chr9:116375023-116375024	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs574498836	chr9:116375033-116375034	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557438402	chr9:116375044-116375045	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs576383238	chr9:116375089-116375090	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs5900056	chr9:116375093-116375094	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs563771156	chr9:116375094-116375095	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs3983376	chr9:116375109-116375110	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192572436	chr9:116375115-116375116	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs28510191	chr9:116375146-116375147	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs561696740	chr9:116375151-116375152	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs372768797	chr9:116375183-116375184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs371079417	chr9:116375301-116375302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs184006306	chr9:116375304-116375305	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs560377125	chr9:116375377-116375378	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs71503569	chr9:116375380-116375381	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs548881071	chr9:116375416-116375417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540723295	chr9:116375427-116375428	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs751709	chr9:116375523-116375524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs140205880	chr9:116375566-116375567	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs545949162	chr9:116375570-116375571	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs187959572	chr9:116375571-116375572	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs569340506	chr9:116375593-116375594	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs529530738	chr9:116375594-116375595	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs59745402	chr9:116375602-116375603	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs549283618	chr9:116375642-116375643	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs566092106	chr9:116375650-116375651	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs535228803	chr9:116375678-116375679	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs559856540	chr9:116375736-116375737	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs74892367	chr9:116375744-116375745	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs143857215	chr9:116375749-116375750	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs571707997	chr9:116375768-116375769	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs537570490	chr9:116375812-116375813	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs564296742	chr9:116375823-116375824	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs144685266	chr9:116375874-116375875	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs531388465	chr9:116375896-116375897	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574097719	chr9:116375925-116375926	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191458579	chr9:116375940-116375941	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs555640167	chr9:116375962-116375963	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572105566	chr9:116375964-116375965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs184666493	chr9:116375965-116375966	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190517001	chr9:116375984-116375985	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs564173513	chr9:116375987-116375988	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs549912486	chr9:116375994-116375995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs181736254	chr9:116376016-116376017	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186636261	chr9:116376038-116376039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs112736082	chr9:116376046-116376047	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs12002107	chr9:116376064-116376065	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:947 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116366200-116375800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr9:116371200-116377800	Weak transcription	Esophagus	oesophagus
3	chr9:116371200-116380200	Enhancers	Fetal Muscle Leg	muscle
4	chr9:116371800-116375400	Enhancers	Pancreas	Pancrea
5	chr9:116371800-116377600	Enhancers	Adipose Nuclei	Adipose
6	chr9:116371800-116379400	Enhancers	Left Ventricle	heart
7	chr9:116372200-116375200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr9:116372200-116376800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr9:116372200-116377000	Weak transcription	Fetal Intestine Large	intestine
10	chr9:116372400-116376200	Weak transcription	Brain Substantia Nigra	brain
11	chr9:116372400-116376400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:116372400-116376400	Weak transcription	Brain Angular Gyrus	brain
13	chr9:116372400-116376400	Weak transcription	NH-A	brain
14	chr9:116372400-116376800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr9:116372400-116376800	Weak transcription	Fetal Intestine Small	intestine
16	chr9:116372400-116377000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr9:116372400-116377000	Weak transcription	HMEC	breast
18	chr9:116372600-116375000	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr9:116372600-116376200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr9:116372600-116376200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr9:116372600-116376200	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr9:116372600-116376200	Weak transcription	Aorta	Aorta
23	chr9:116372600-116376200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr9:116372600-116376200	Weak transcription	Colon Smooth Muscle	Colon
25	chr9:116372600-116376800	Weak transcription	Brain Cingulate Gyrus	brain
26	chr9:116372600-116376800	Weak transcription	Osteobl	bone
27	chr9:116372600-116377000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr9:116372600-116377200	Weak transcription	Brain Anterior Caudate	brain
29	chr9:116372800-116375600	Weak transcription	HSMM	muscle
30	chr9:116372800-116376200	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr9:116372800-116376200	Weak transcription	Ovary	ovary
32	chr9:116372800-116376600	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr9:116372800-116376600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr9:116372800-116379400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr9:116373000-116376200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr9:116373000-116376200	Weak transcription	Fetal Lung	lung
37	chr9:116373000-116376400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr9:116373000-116376400	Weak transcription	Stomach Mucosa	stomach
39	chr9:116373000-116376400	Enhancers	HepG2	liver
40	chr9:116373200-116376400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:116373200-116376600	Weak transcription	Brain Hippocampus Middle	brain
42	chr9:116373200-116376800	Weak transcription	Stomach Smooth Muscle	stomach
43	chr9:116373200-116377400	Weak transcription	Psoas Muscle	Psoas
44	chr9:116373400-116375200	Weak transcription	Right Ventricle	heart
45	chr9:116373400-116375400	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr9:116373400-116375600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr9:116373400-116375800	Weak transcription	Lung	lung
48	chr9:116373400-116376400	Weak transcription	Right Atrium	heart
49	chr9:116373400-116377000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr9:116373400-116377000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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