Variant report

Variant	nsv963301
Chromosome Location	chr3:19992240-19993486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:13)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:13 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr3:19993093-19993118	GM10266	blood:	n/a	n/a
2	CUX1	chr3:19992276-19992285	GM12878	blood:	n/a	n/a
3	POLR2A	chr3:19986265-20000717	K562	blood:	n/a	n/a
4	POLR2A	chr3:19993248-19993310	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr3:19993139-19993150	MCF-7	breast:	n/a	n/a
6	POLR2A	chr3:19993061-19993261	MCF10A-Er-Src	breast:	n/a	n/a
7	POLR2A	chr3:19993460-19993646	HepG2	liver:	n/a	n/a
8	POLR2A	chr3:19993409-19993815	MCF10A-Er-Src	breast:	n/a	n/a
9	POLR2A	chr3:19993343-19993893	GM12878	blood:	n/a	n/a
10	STAT3	chr3:19992351-19992520	MCF10A-Er-Src	breast:	n/a	n/a
11	STAT3	chr3:19992442-19992470	MCF10A-Er-Src	breast:	n/a	n/a
12	TAF7	chr3:19992979-19993295	H1-hESC	embryonic stem cell:	n/a	n/a
13	ZNF384	chr3:19993006-19993365	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:19992400-19992450	HRE	kidney:	n/a
2	chr3:19992400-19992450	Jurkat	blood:	n/a
3	chr3:19992400-19992450	HUVEC	blood vessel:	n/a
4	chr3:19992400-19992450	GM12878	blood:	n/a
5	chr3:19992400-19992450	PFSK-1	brain:	n/a
6	chr3:19992400-19992450	AG04449	skin:	fetal
7	chr3:19992400-19992450	SAEC	small airway:	n/a
8	chr3:19992400-19992450	H1-hESC	embryonic stem cell:	embryo
9	chr3:19992400-19992450	HEEpiC	esophagus:	n/a
10	chr3:19992400-19992450	HEK293	kidney:	embryo
11	chr3:19992400-19992450	HL-60	blood:	n/a
12	chr3:19992400-19992450	RPTEC	kidney:	n/a
13	chr3:19992400-19992450	HRPEpiC	eye:	n/a
14	chr3:19992400-19992450	NB4	blood:	n/a
15	chr3:19992400-19992450	NH-A	brain:	n/a
16	chr3:19992400-19992450	ProgFib	skin:	n/a
17	chr3:19992400-19992450	AG09319	gingival:	n/a
18	chr3:19992400-19992450	ovcar-3	ovarian:	n/a
19	chr3:19992400-19992450	AG04450	lung:	fetal
20	chr3:19992400-19992450	BJ	skin:	n/a
21	chr3:19992400-19992450	A549	lung:	n/a
22	chr3:19992400-19992450	HNPCEpiC	eye:	n/a
23	chr3:19992400-19992450	Hepatocyte	liver:	n/a
24	chr3:19992400-19992450	T-47D	breast:	n/a
25	chr3:19992400-19992450	HRCEpiC	kidney:	n/a
26	chr3:19992400-19992450	NHDF-neo	bronchial:	n/a
27	chr3:19992400-19992450	Caco-2	colon:	n/a
28	chr3:19992400-19992450	HCF	heart:	n/a
29	chr3:19992400-19992450	GM12891	blood:	n/a
30	chr3:19992400-19992450	GM12892	blood:	n/a
31	chr3:19992400-19992450	NHBE	bronchial:	n/a
32	chr3:19992400-19992450	PrEC	prostate:	n/a
33	chr3:19992400-19992450	HepG2	liver:	n/a
34	chr3:19992400-19992450	LNCaP	prostate:	n/a
35	chr3:19992400-19992450	HCPEpiC	choroid plexus:	n/a
36	chr3:19992400-19992450	PANC-1	pancreas:	n/a
37	chr3:19992400-19992450	HMEC	breast:	n/a
38	chr3:19992400-19992450	MCF10A-Er-Src	breast:	n/a
39	chr3:19992400-19992450	SK-N-SH	brain:	n/a
40	chr3:19992400-19992450	HPAEpiC	pulmonary alveolar:	n/a
41	chr3:19992400-19992450	SK-N-SH_RA	brain:	n/a
42	chr3:19992400-19992450	NT2-D1	testis:	n/a
43	chr3:19992400-19992450	HCT-116	colon:	n/a
44	chr3:19992400-19992450	IMR90	lung:	fetal
45	chr3:19992400-19992450	MCF-7	breast:	n/a
46	chr3:19992400-19992450	SK-N-MC	brain:	n/a
47	chr3:19992400-19992450	GM06990	blood:	n/a
48	chr3:19992400-19992450	U87	brain:	n/a
49	chr3:19992400-19992450	AG09309	skin:	n/a
50	chr3:19992400-19992450	HIPEpiC	eye:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:19991110..19993492-chr3:20053410..20056377,2	K562	blood:
2	chr3:19992532..19994138-chr3:20013293..20015192,2	K562	blood:
3	chr3:19971502..19973500-chr3:19993301..19994870,2	K562	blood:
4	chr3:19987439..19992261-chr3:20226257..20229350,4	K562	blood:
5	chr3:19986985..19992254-chr3:20079680..20083856,14	K562	blood:
6	chr3:19986921..19992254-chr3:20078952..20084327,16	K562	blood:
7	chr3:19987383..19992426-chr3:20011245..20019650,13	MCF-7	breast:

No data

Variant related genes	Relation type
EFHB	TF binding region
RAB5A	TF binding region
EFHB	CpG island
RAB5A	CpG island
ENSG00000144566	chromatin interactions
ENSG00000129810	chromatin interactions
ENSG00000229468	chromatin interactions
ENSG00000183977	chromatin interactions
ENSG00000114166	chromatin interactions

Extended variants
information (count: 72 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:72 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189794197	chr3:19992265-19992266	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs543002874	chr3:19992277-19992278	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs369479155	chr3:19992294-19992295	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs11717172	chr3:19992312-19992313	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs532008844	chr3:19992338-19992339	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs371868725	chr3:19992343-19992344	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs115981030	chr3:19992388-19992389	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs200047397	chr3:19992401-19992402	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs111819761	chr3:19992405-19992406	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs144198452	chr3:19992406-19992407	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs139006514	chr3:19992422-19992423	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs149206559	chr3:19992430-19992431	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs6773437	chr3:19992432-19992433	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs11545950	chr3:19992444-19992445	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs147139196	chr3:19992445-19992446	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs149313297	chr3:19992456-19992457	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs35986369	chr3:19992467-19992468	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs148447810	chr3:19992477-19992478	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs201114014	chr3:19992552-19992553	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs374073544	chr3:19992580-19992581	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs10510496	chr3:19992588-19992589	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs180981510	chr3:19992592-19992593	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs577905094	chr3:19992655-19992656	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs186445429	chr3:19992698-19992699	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs553693581	chr3:19992709-19992710	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs572457175	chr3:19992743-19992744	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs543159268	chr3:19992765-19992766	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs561402866	chr3:19992766-19992767	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs577249590	chr3:19992802-19992803	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs116804152	chr3:19992812-19992813	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs559755999	chr3:19992818-19992819	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs56994247	chr3:19992901-19992902	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs191346037	chr3:19992916-19992917	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs532705834	chr3:19992917-19992918	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs547925566	chr3:19992919-19992920	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs183649860	chr3:19992946-19992947	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs187517948	chr3:19992948-19992949	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs548650765	chr3:19992978-19992979	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs572086749	chr3:19992986-19992987	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs59608170	chr3:19993083-19993084	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs34843691	chr3:19993115-19993116	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs35519937	chr3:19993130-19993131	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs34525091	chr3:19993133-19993134	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs35838380	chr3:19993149-19993150	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs537443984	chr3:19993153-19993154	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs549405615	chr3:19993164-19993165	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs571478178	chr3:19993172-19993173	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs538558923	chr3:19993181-19993182	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs544145402	chr3:19993194-19993195	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs199594518	chr3:19993200-19993201	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:19989800-19993000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:19989800-19993000	Weak transcription	Esophagus	oesophagus
3	chr3:19989800-19993000	Weak transcription	Spleen	Spleen
4	chr3:19989800-19995000	Weak transcription	Gastric	stomach
5	chr3:19989800-20018800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:19990000-19992600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr3:19990000-19993400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr3:19990000-20008600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr3:19990000-20016200	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr3:19990800-19992400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr3:19990800-19993000	Weak transcription	Fetal Stomach	stomach
12	chr3:19990800-19996600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
13	chr3:19990800-20017000	Weak transcription	Fetal Kidney	kidney
14	chr3:19991000-19992400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr3:19991000-19992400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:19991000-19992400	Active TSS	GM12878-XiMat	blood
17	chr3:19991000-19992600	Weak transcription	HSMM	muscle
18	chr3:19991000-19993000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr3:19991000-19993000	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr3:19991000-19993000	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr3:19991000-19993000	Weak transcription	Right Atrium	heart
22	chr3:19991000-19993000	Weak transcription	Thymus	Thymus
23	chr3:19991000-19993200	Weak transcription	Brain Hippocampus Middle	brain
24	chr3:19991000-19993200	Weak transcription	HSMMtube	muscle
25	chr3:19991000-19995200	Weak transcription	Brain Germinal Matrix	brain
26	chr3:19991000-19996200	Weak transcription	Colon Smooth Muscle	Colon
27	chr3:19991000-19996600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr3:19991000-20001800	Weak transcription	Brain Angular Gyrus	brain
29	chr3:19991200-19992400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr3:19991200-19992400	Weak transcription	Osteobl	bone
31	chr3:19991200-19992600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr3:19991200-19992800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr3:19991200-19993000	Weak transcription	Brain Anterior Caudate	brain
34	chr3:19991200-19993200	Weak transcription	Primary B cells from cord blood	blood
35	chr3:19991200-20002600	Weak transcription	Fetal Heart	heart
36	chr3:19991400-19992400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr3:19991400-19992400	Weak transcription	Duodenum Mucosa	Duodenum
38	chr3:19991400-19992400	Active TSS	NHLF	lung
39	chr3:19991400-19992600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr3:19991400-19992800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr3:19991400-19992800	Weak transcription	Fetal Brain Male	brain
42	chr3:19991400-19993000	Weak transcription	Fetal Muscle Trunk	muscle
43	chr3:19991400-19993000	Weak transcription	Stomach Smooth Muscle	stomach
44	chr3:19991400-19993200	Weak transcription	Right Ventricle	heart
45	chr3:19991400-19993800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr3:19991400-19995000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr3:19991400-19995400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr3:19991400-19995400	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr3:19991400-19998200	Weak transcription	Aorta	Aorta
50	chr3:19991400-19998800	Strong transcription	Fetal Thymus	thymus

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