Variant report

Variant	nsv961914
Chromosome Location	chr2:178481282-178483895
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:465)
CpG islands
(count:427)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:465 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:178483392-178484091	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:178483586-178484172	K562	blood:	n/a	n/a
3	ATF2	chr2:178483240-178483882	GM12878	blood:	n/a	n/a
4	ATF3	chr2:178483528-178483847	K562	blood:	n/a	n/a
5	ATF3	chr2:178483541-178483773	GM12878	blood:	n/a	n/a
6	ATF3	chr2:178483568-178483887	HepG2	liver:	n/a	n/a
7	BACH1	chr2:178483373-178483887	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr2:178483115-178484098	A549	lung:	n/a	n/a
9	BCL3	chr2:178483225-178484132	A549	lung:	n/a	n/a
10	BCLAF1	chr2:178483181-178483981	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:178483421-178483940	HepG2	liver:	n/a	n/a
12	BHLHE40	chr2:178483296-178483938	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:178483301-178484100	K562	blood:	n/a	n/a
14	BRCA1	chr2:178483333-178483912	HepG2	liver:	n/a	n/a
15	CBX3	chr2:178482690-178484232	K562	blood:	n/a	n/a
16	CCNT2	chr2:178483310-178483872	K562	blood:	n/a	n/a
17	CEBPB	chr2:178483473-178483808	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr2:178483459-178483919	HepG2	liver:	n/a	n/a
19	CEBPD	chr2:178483538-178483932	HepG2	liver:	n/a	n/a
20	CHD1	chr2:178483275-178483525	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr2:178483251-178483993	GM12878	blood:	n/a	n/a
22	CHD2	chr2:178483253-178484002	GM12878	blood:	n/a	n/a
23	CHD2	chr2:178483290-178483925	K562	blood:	n/a	n/a
24	CHD2	chr2:178483318-178483978	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr2:178483313-178483853	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr2:178483281-178483998	HepG2	liver:	n/a	n/a
27	CREB1	chr2:178483248-178483953	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr2:178483290-178483999	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr2:178483378-178483852	A549	lung:	n/a	n/a
30	CREB1	chr2:178483265-178484106	HepG2	liver:	n/a	n/a
31	CREB1	chr2:178483254-178483890	A549	lung:	n/a	n/a
32	CTCF	chr2:178483560-178483710	NHLF	lung:	n/a	n/a
33	CTCF	chr2:178483740-178483890	GM12864	blood:	n/a	n/a
34	CTCF	chr2:178483720-178483870	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr2:178483380-178483530	GM12871	blood:	n/a	n/a
36	CTCF	chr2:178483300-178483450	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr2:178483320-178483470	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr2:178483687-178483856	Fibrobl	skin:	n/a	n/a
39	CTCF	chr2:178483340-178483490	GM12873	blood:	n/a	n/a
40	CTCF	chr2:178483700-178483850	HepG2	liver:	n/a	n/a
41	CTCF	chr2:178483709-178483793	MCF-7	breast:	n/a	n/a
42	CTCF	chr2:178483264-178483295	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr2:178483280-178483430	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr2:178483688-178483786	GM12891	blood:	n/a	n/a
45	CTCF	chr2:178483340-178483490	HAc	cerebellar:	n/a	n/a
46	CTCF	chr2:178483300-178483450	HCFaa	heart:	n/a	n/a
47	CTCF	chr2:178483679-178483836	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:178483702-178483790	GM19239	blood:	n/a	n/a
49	CTCF	chr2:178483760-178483796	A549	lung:	n/a	n/a
50	CTCF	chr2:178483660-178483810	SAEC	small airway:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:178483411-178483461	ovcar-3	ovarian:	n/a
2	chr2:178482258-178482308	HEEpiC	esophagus:	n/a
3	chr2:178483847-178483897	Hepatocyte	liver:	n/a
4	chr2:178483847-178483897	HRPEpiC	eye:	n/a
5	chr2:178483847-178483897	HAEpiC	amniotic membrane:	n/a
6	chr2:178483847-178483897	AG04450	lung:	fetal
7	chr2:178483882-178483932	PrEC	prostate:	n/a
8	chr2:178482258-178482308	HIPEpiC	eye:	n/a
9	chr2:178483601-178483651	GM06990	blood:	n/a
10	chr2:178483498-178483548	HEK293	kidney:	embryo
11	chr2:178483882-178483932	MCF-7	breast:	n/a
12	chr2:178483498-178483548	HRPEpiC	eye:	n/a
13	chr2:178483498-178483548	HCM	heart:	n/a
14	chr2:178483601-178483651	PFSK-1	brain:	n/a
15	chr2:178483601-178483651	BJ	skin:	n/a
16	chr2:178483847-178483897	HCPEpiC	choroid plexus:	n/a
17	chr2:178483601-178483651	HUVEC	blood vessel:	n/a
18	chr2:178482258-178482308	Hela-S3	cervix:	n/a
19	chr2:178483411-178483461	H1-hESC	embryonic stem cell:	embryo
20	chr2:178481527-178481577	HEK293	kidney:	embryo
21	chr2:178483498-178483548	AG09309	skin:	n/a
22	chr2:178481527-178481577	GM12892	blood:	n/a
23	chr2:178483498-178483548	HCF	heart:	n/a
24	chr2:178483847-178483897	HUVEC	blood vessel:	n/a
25	chr2:178483847-178483897	HIPEpiC	eye:	n/a
26	chr2:178483498-178483548	PANC-1	pancreas:	n/a
27	chr2:178483498-178483548	HCPEpiC	choroid plexus:	n/a
28	chr2:178483847-178483897	AG04449	skin:	fetal
29	chr2:178483882-178483932	AG09309	skin:	n/a
30	chr2:178483847-178483897	ovcar-3	ovarian:	n/a
31	chr2:178483498-178483548	ovcar-3	ovarian:	n/a
32	chr2:178483498-178483548	T-47D	breast:	n/a
33	chr2:178483601-178483651	HCPEpiC	choroid plexus:	n/a
34	chr2:178483498-178483548	HRE	kidney:	n/a
35	chr2:178483882-178483932	GM12891	blood:	n/a
36	chr2:178483601-178483651	ECC-1	luminal epithelium:	n/a
37	chr2:178483847-178483897	GM12891	blood:	n/a
38	chr2:178483882-178483932	ovcar-3	ovarian:	n/a
39	chr2:178483601-178483651	SKMC	muscle:	n/a
40	chr2:178483411-178483461	PANC-1	pancreas:	n/a
41	chr2:178483882-178483932	HepG2	liver:	n/a
42	chr2:178483498-178483548	HPAEpiC	pulmonary alveolar:	n/a
43	chr2:178483411-178483461	SK-N-MC	brain:	n/a
44	chr2:178483882-178483932	ProgFib	skin:	n/a
45	chr2:178483847-178483897	SAEC	small airway:	n/a
46	chr2:178482258-178482308	HAEpiC	amniotic membrane:	n/a
47	chr2:178483411-178483461	HEEpiC	esophagus:	n/a
48	chr2:178483601-178483651	A549	lung:	n/a
49	chr2:178483882-178483932	CMK	blood:	n/a
50	chr2:178483882-178483932	GM19239	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:178255830..178259425-chr2:178483453..178485926,4	K562	blood:
2	chr2:178480859..178483355-chr2:178499342..178501117,2	K562	blood:
3	chr2:178479040..178481545-chr2:178589525..178591056,2	K562	blood:
4	chr2:178415963..178418015-chr2:178480825..178484170,3	K562	blood:
5	chr2:178416378..178418708-chr2:178482397..178484777,2	MCF-7	breast:
6	chr2:178076328..178078766-chr2:178482248..178484815,2	K562	blood:
7	chr2:178406620..178408509-chr2:178480094..178481704,2	K562	blood:
8	chr2:178479419..178481320-chr2:178491408..178493665,2	K562	blood:

No data

Variant related genes	Relation type
TTC30A	TF binding region
TTC30A	CpG island
ENSG00000170144	chromatin interactions
ENSG00000229337	chromatin interactions
ENSG00000213963	chromatin interactions
ENSG00000116044	chromatin interactions
ENSG00000018510	chromatin interactions
ENSG00000263721	chromatin interactions
ENSG00000196659	chromatin interactions

Extended variants
information (count: 167 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:167 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558947109	chr2:178481308-178481309	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs16865451	chr2:178481325-178481326	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs537871944	chr2:178481344-178481345	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550409444	chr2:178481373-178481374	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs202031677	chr2:178481391-178481392	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368688803	chr2:178481392-178481393	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs141579721	chr2:178481394-178481395	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs57691380	chr2:178481399-178481400	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs138508100	chr2:178481419-178481420	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs368497661	chr2:178481424-178481425	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148134162	chr2:178481433-178481434	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs145161761	chr2:178481440-178481441	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs201002476	chr2:178481447-178481448	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143980990	chr2:178481449-178481450	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs139052986	chr2:178481462-178481463	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs140497773	chr2:178481527-178481528	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs147824426	chr2:178481528-178481529	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs139721706	chr2:178481546-178481547	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs151240685	chr2:178481566-178481567	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145281774	chr2:178481620-178481621	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs376314961	chr2:178481629-178481630	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs141300543	chr2:178481642-178481643	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs368671519	chr2:178481647-178481648	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs554097020	chr2:178481658-178481659	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs199946796	chr2:178481687-178481688	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs17854236	chr2:178481700-178481701	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs2717526	chr2:178481705-178481706	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs2717527	chr2:178481708-178481709	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs200143704	chr2:178481714-178481715	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs201182703	chr2:178481741-178481742	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs142220180	chr2:178481747-178481748	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs143835014	chr2:178481753-178481754	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs200192095	chr2:178481775-178481776	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs150534803	chr2:178481798-178481799	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369981799	chr2:178481805-178481806	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs10497497	chr2:178481818-178481819	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs61747539	chr2:178481821-178481822	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373577016	chr2:178481838-178481839	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370009389	chr2:178481951-178481952	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs372657538	chr2:178481954-178481955	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201394288	chr2:178482035-178482036	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144179180	chr2:178482079-178482080	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs199542168	chr2:178482088-178482089	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs28630685	chr2:178482094-178482095	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576401783	chr2:178482101-178482102	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs541881631	chr2:178482106-178482107	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs551143270	chr2:178482216-178482217	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs555446019	chr2:178482219-178482220	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2953467	chr2:178482221-178482222	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs572302566	chr2:178482222-178482223	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

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
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178462800-178482800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:178464200-178482600	Weak transcription	Psoas Muscle	Psoas
3	chr2:178464200-178482600	Weak transcription	Stomach Smooth Muscle	stomach
4	chr2:178464600-178482400	Weak transcription	Colon Smooth Muscle	Colon
5	chr2:178468400-178482800	Weak transcription	Fetal Brain Male	brain
6	chr2:178471800-178482600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr2:178476400-178482800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr2:178476800-178482600	Weak transcription	HepG2	liver
9	chr2:178477400-178482600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr2:178477600-178482600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr2:178477800-178482400	Weak transcription	Brain Substantia Nigra	brain
12	chr2:178477800-178482800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr2:178477800-178482800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr2:178479600-178482600	Weak transcription	HSMM	muscle
15	chr2:178480000-178482600	Weak transcription	K562	blood
16	chr2:178480000-178482800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr2:178480800-178481800	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr2:178481000-178481400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr2:178481000-178481400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
20	chr2:178481000-178481400	Active TSS	Fetal Lung	lung
21	chr2:178481000-178481600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr2:178481000-178481600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr2:178481000-178481600	ZNF genes & repeats	Fetal Kidney	kidney
24	chr2:178481200-178481400	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr2:178481200-178482200	Weak transcription	Right Ventricle	heart
26	chr2:178481200-178482600	Weak transcription	Brain Angular Gyrus	brain
27	chr2:178481200-178482600	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr2:178481200-178482600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr2:178481200-178482600	Weak transcription	Left Ventricle	heart
30	chr2:178481200-178482600	Weak transcription	Ovary	ovary
31	chr2:178481200-178482600	Weak transcription	Pancreas	Pancrea
32	chr2:178481200-178482600	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr2:178481200-178482600	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr2:178481200-178482800	Weak transcription	Gastric	stomach
35	chr2:178481200-178482800	Weak transcription	Right Atrium	heart
36	chr2:178481200-178482800	Weak transcription	GM12878-XiMat	blood
37	chr2:178481400-178481600	Enhancers	Fetal Heart	heart
38	chr2:178481400-178482600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr2:178481400-178482600	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr2:178481400-178482600	Weak transcription	Fetal Lung	lung
41	chr2:178481400-178482600	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr2:178481600-178482200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr2:178481600-178482600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:178481600-178482600	Weak transcription	Fetal Heart	heart
45	chr2:178481600-178482800	Weak transcription	Fetal Kidney	kidney
46	chr2:178481800-178482800	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr2:178482200-178482600	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr2:178482200-178482800	Enhancers	Right Ventricle	heart
49	chr2:178482400-178482600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:178482400-178482600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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