Variant report

Variant	esv3458778
Chromosome Location	chr2:179309167-179312263
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:31)
CpG islands
(count:123)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:31 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr2:179311281-179311393	HepG2	liver:	n/a	n/a
2	GATA3	chr2:179309174-179309446	SH-SY5Y	brain:	n/a	n/a
3	JUN	chr2:179309133-179309186	K562	blood:	n/a	n/a
4	MAFF	chr2:179312188-179312213	K562	blood:	n/a	n/a
5	MAFK	chr2:179310165-179310367	HepG2	liver:	n/a	chr2:179310300-179310315
6	MAFK	chr2:179310215-179310388	HepG2	liver:	n/a	chr2:179310300-179310315
7	NFYB	chr2:179309048-179309298	GM12878	blood:	n/a	n/a
8	POLR2A	chr2:179311898-179312050	K562	blood:	n/a	n/a
9	POLR2A	chr2:179310940-179311400	HepG2	liver:	n/a	n/a
10	POLR2A	chr2:179311078-179311162	ProgFib	skin:	n/a	n/a
11	POLR2A	chr2:179312128-179312210	MCF10A-Er-Src	breast:	n/a	n/a
12	POLR2A	chr2:179310128-179310551	HepG2	liver:	n/a	n/a
13	POLR2A	chr2:179310039-179310467	HepG2	liver:	n/a	n/a
14	POLR2A	chr2:179311051-179311371	HepG2	liver:	n/a	n/a
15	POLR2A	chr2:179310377-179310504	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr2:179311106-179311416	HepG2	liver:	n/a	n/a
17	POLR2A	chr2:179311195-179311203	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr2:179311959-179312360	HepG2	liver:	n/a	n/a
19	POLR2A	chr2:179311177-179311409	GM12891	blood:	n/a	n/a
20	POLR2A	chr2:179310232-179310531	GM12878	blood:	n/a	n/a
21	POLR2A	chr2:179310557-179310860	HepG2	liver:	n/a	n/a
22	POLR2A	chr2:179309144-179310551	HepG2	liver:	n/a	n/a
23	POLR2A	chr2:179311050-179311192	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr2:179311184-179311198	ProgFib	skin:	n/a	n/a
25	POLR2A	chr2:179310370-179310406	MCF-7	breast:	n/a	n/a
26	POLR2A	chr2:179312228-179312251	MCF10A-Er-Src	breast:	n/a	n/a
27	POLR2A	chr2:179310163-179310561	K562	blood:	n/a	n/a
28	POLR2A	chr2:179311169-179311181	ProgFib	skin:	n/a	n/a
29	POLR2A	chr2:179311046-179311459	K562	blood:	n/a	n/a
30	POLR2A	chr2:179310159-179310277	HepG2	liver:	n/a	n/a
31	POLR2A	chr2:179310317-179310678	GM12891	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:179310165-179310215	HAEpiC	amniotic membrane:	n/a
2	chr2:179310165-179310215	HAEpiC	amniotic membrane:	n/a
3	chr2:179310165-179310215	HMEC	breast:	n/a
4	chr2:179309384-179309434	HCT-116	colon:	n/a
5	chr2:179309384-179309434	U87	brain:	n/a
6	chr2:179309384-179309434	HUVEC	blood vessel:	n/a
7	chr2:179310165-179310215	SK-N-MC	brain:	n/a
8	chr2:179310165-179310215	ECC-1	luminal epithelium:	n/a
9	chr2:179310165-179310215	BJ	skin:	n/a
10	chr2:179310165-179310215	AG04450	lung:	fetal
11	chr2:179310165-179310215	PANC-1	pancreas:	n/a
12	chr2:179310165-179310215	NHBE	bronchial:	n/a
13	chr2:179309384-179309434	HNPCEpiC	eye:	n/a
14	chr2:179309384-179309434	AG09309	skin:	n/a
15	chr2:179309384-179309434	SK-N-MC	brain:	n/a
16	chr2:179310165-179310215	Jurkat	blood:	n/a
17	chr2:179309384-179309434	LNCaP	prostate:	n/a
18	chr2:179310165-179310215	NHDF-neo	bronchial:	n/a
19	chr2:179310165-179310215	IMR90	lung:	fetal
20	chr2:179310165-179310215	U87	brain:	n/a
21	chr2:179310165-179310215	HepG2	liver:	n/a
22	chr2:179309384-179309434	NHDF-neo	bronchial:	n/a
23	chr2:179310165-179310215	AG04449	skin:	fetal
24	chr2:179310165-179310215	HNPCEpiC	eye:	n/a
25	chr2:179310165-179310215	HRE	kidney:	n/a
26	chr2:179310165-179310215	SK-N-SH	brain:	n/a
27	chr2:179309384-179309434	HPAEpiC	pulmonary alveolar:	n/a
28	chr2:179310165-179310215	HUVEC	blood vessel:	n/a
29	chr2:179309384-179309434	SKMC	muscle:	n/a
30	chr2:179310165-179310215	K562	blood:	n/a
31	chr2:179309384-179309434	HEEpiC	esophagus:	n/a
32	chr2:179309384-179309434	GM12892	blood:	n/a
33	chr2:179309384-179309434	SAEC	small airway:	n/a
34	chr2:179310165-179310215	AG09319	gingival:	n/a
35	chr2:179310165-179310215	MCF-7	breast:	n/a
36	chr2:179310165-179310215	PrEC	prostate:	n/a
37	chr2:179309384-179309434	AG09319	gingival:	n/a
38	chr2:179309384-179309434	Hepatocyte	liver:	n/a
39	chr2:179310165-179310215	HIPEpiC	eye:	n/a
40	chr2:179310165-179310215	SAEC	small airway:	n/a
41	chr2:179309384-179309434	CMK	blood:	n/a
42	chr2:179310165-179310215	NB4	blood:	n/a
43	chr2:179310165-179310215	HRPEpiC	eye:	n/a
44	chr2:179309384-179309434	HMEC	breast:	n/a
45	chr2:179310165-179310215	GM19239	blood:	n/a
46	chr2:179310165-179310215	NH-A	brain:	n/a
47	chr2:179309384-179309434	HEK293	kidney:	embryo
48	chr2:179310165-179310215	HCPEpiC	choroid plexus:	n/a
49	chr2:179309384-179309434	HCPEpiC	choroid plexus:	n/a
50	chr2:179310165-179310215	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:179311363..179318324-chr2:179340414..179346232,28	K562	blood:
2	chr2:179311612..179313781-chr2:179328660..179331380,2	K562	blood:
3	chr2:179310863..179318324-chr2:179338966..179346608,29	K562	blood:
4	chr2:179309273..179312087-chr2:179344521..179346573,2	MCF-7	breast:
5	chr2:179308416..179311292-chr2:179342166..179344945,2	MCF-7	breast:
6	chr2:179312045..179317660-chr2:179337933..179347437,24	MCF-7	breast:
7	chr2:179276988..179281129-chr2:179311895..179317764,7	MCF-7	breast:

No data

Variant related genes	Relation type
PRKRA	TF binding region
DFNB59	TF binding region
PRKRA	CpG island
DFNB59	CpG island
ENSG00000079150	chromatin interactions
ENSG00000223960	chromatin interactions
ENSG00000116095	chromatin interactions

Extended variants
information (count: 105 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151157679	chr2:179309210-179309211	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs373977506	chr2:179309229-179309230	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs61744874	chr2:179309245-179309246	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs201120161	chr2:179309272-179309273	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537508647	chr2:179309292-179309293	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs551107215	chr2:179309303-179309304	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs567632860	chr2:179309308-179309309	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs147609208	chr2:179309314-179309315	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs553436384	chr2:179309325-179309326	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs377150141	chr2:179309328-179309329	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs534495063	chr2:179309333-179309334	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs573471150	chr2:179309357-179309358	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs142115054	chr2:179309377-179309378	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs559059299	chr2:179309385-179309386	Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs575758053	chr2:179309398-179309399	Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs543078967	chr2:179309474-179309475	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs74387294	chr2:179309477-179309478	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs370029277	chr2:179309484-179309485	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs554549119	chr2:179309543-179309544	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs188539194	chr2:179309608-179309609	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs181328404	chr2:179309617-179309618	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs528384166	chr2:179309633-179309634	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs574044733	chr2:179309701-179309702	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs551392513	chr2:179309737-179309738	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs565052673	chr2:179309779-179309780	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs34109663	chr2:179309783-179309784	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs62176110	chr2:179309910-179309911	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs144297360	chr2:179310049-179310050	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs551068517	chr2:179310078-179310079	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs536663881	chr2:179310085-179310086	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs3216708	chr2:179310086-179310087	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs397871146	chr2:179310095-179310096	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs567744710	chr2:179310140-179310141	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs151159317	chr2:179310152-179310153	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs536781153	chr2:179310158-179310159	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs547010375	chr2:179310165-179310166	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs185477394	chr2:179310313-179310314	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs372138881	chr2:179310376-179310377	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs189059046	chr2:179310392-179310393	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs539279533	chr2:179310496-179310497	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs140098008	chr2:179310620-179310621	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs569404273	chr2:179310648-179310649	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs538027007	chr2:179310665-179310666	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs554778669	chr2:179310678-179310679	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs115662402	chr2:179310765-179310766	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs150290481	chr2:179310782-179310783	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs552887470	chr2:179310786-179310787	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs572763316	chr2:179310793-179310794	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs180967255	chr2:179310798-179310799	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs565057501	chr2:179310828-179310829	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Schizophrenia	19348701	CNVD
Muscular dystrophy	17160897	CNVD
Cardiomyopathy	17576883	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179279800-179313800	Weak transcription	Stomach Mucosa	stomach
2	chr2:179280000-179310600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr2:179280200-179314600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:179290200-179312800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:179290800-179312000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr2:179290800-179312600	Strong transcription	Dnd41	blood
7	chr2:179291000-179311600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:179291000-179313200	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr2:179291000-179313400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr2:179291000-179313600	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr2:179291200-179310400	Strong transcription	Primary B cells from peripheral blood	blood
12	chr2:179291200-179312200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr2:179291200-179312800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr2:179291200-179312800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:179291200-179312800	Strong transcription	Skeletal Muscle Female	skeletal muscle
16	chr2:179291200-179313600	Strong transcription	Fetal Thymus	thymus
17	chr2:179291200-179313800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr2:179291400-179311400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr2:179291400-179312600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr2:179291400-179312800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:179291400-179313400	Strong transcription	HSMM	muscle
22	chr2:179291400-179313600	Strong transcription	Rectal Mucosa Donor 29	rectum
23	chr2:179291600-179312600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr2:179291600-179312800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:179291600-179312800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr2:179291600-179313200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr2:179291600-179313400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
28	chr2:179291600-179313600	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr2:179291800-179313000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:179291800-179314000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:179292000-179314600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr2:179292400-179312800	Weak transcription	Fetal Heart	heart
33	chr2:179293200-179312600	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr2:179293600-179313000	Strong transcription	Liver	Liver
35	chr2:179293800-179310200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr2:179293800-179313600	Strong transcription	Adipose Nuclei	Adipose
37	chr2:179293800-179313800	Strong transcription	HUVEC	blood vessel
38	chr2:179294000-179313000	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr2:179294200-179314200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
40	chr2:179295400-179311000	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr2:179295400-179311600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr2:179295400-179312800	Strong transcription	HepG2	liver
43	chr2:179295400-179313600	Strong transcription	Fetal Intestine Large	intestine
44	chr2:179295400-179314000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr2:179297000-179313200	Weak transcription	Right Atrium	heart
46	chr2:179298400-179310200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr2:179298600-179314400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr2:179299600-179310000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:179299600-179314800	Weak transcription	Small Intestine	intestine
50	chr2:179300000-179310400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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