Variant report

Variant	nsv818083
Chromosome Location	chr2:133277683-133308636
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:133304875-133304890	K562	blood:	n/a	n/a
2	ARID3A	chr2:133304775-133304963	HepG2	liver:	n/a	n/a
3	CEBPB	chr2:133280625-133280665	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr2:133304678-133304962	ECC-1	luminal epithelium:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
5	CTCF	chr2:133304460-133304610	K562	blood:	n/a	n/a
6	CTCF	chr2:133304643-133304986	Gliobla	brain:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
7	CTCF	chr2:133289519-133289552	GM13976	blood:	n/a	n/a
8	CTCF	chr2:133304800-133304950	AG10803	skin:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
9	CTCF	chr2:133296860-133297010	GM12869	blood:	n/a	n/a
10	CTCF	chr2:133304748-133304985	HepG2	liver:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
11	CTCF	chr2:133304800-133304950	HCT-116	colon:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
12	CTCF	chr2:133304740-133304890	GM06990	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
13	CTCF	chr2:133304796-133304955	GM12891	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
14	CTCF	chr2:133304800-133304950	HMEC	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
15	CTCF	chr2:133304740-133304890	HCM	heart:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
16	CTCF	chr2:133304780-133304930	SAEC	small airway:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
17	CTCF	chr2:133304140-133304290	AG04450	lung:	n/a	n/a
18	CTCF	chr2:133304780-133304930	AG10803	skin:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
19	CTCF	chr2:133304760-133304910	GM12873	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
20	CTCF	chr2:133304720-133304870	HVMF	connective:	n/a	chr2:133304857-133304870 chr2:133304857-133304866
21	CTCF	chr2:133304800-133304950	AG09319	gingival:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
22	CTCF	chr2:133304760-133304910	NHEK	skin:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
23	CTCF	chr2:133304800-133304950	HEEpiC	esophagus:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
24	CTCF	chr2:133304840-133304990	HCM	heart:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
25	CTCF	chr2:133304780-133304930	HUVEC	blood vessel:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
26	CTCF	chr2:133304820-133304970	AG09309	skin:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
27	CTCF	chr2:133304800-133304950	HAc	cerebellar:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
28	CTCF	chr2:133304760-133304910	HCT-116	colon:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
29	CTCF	chr2:133304733-133304965	A549	lung:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
30	CTCF	chr2:133304785-133304966	MCF-7	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
31	CTCF	chr2:133289569-133289639	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr2:133304780-133304930	GM12869	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
33	CTCF	chr2:133304380-133304530	GM12864	blood:	n/a	n/a
34	CTCF	chr2:133304780-133304930	GM12874	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
35	CTCF	chr2:133304760-133304910	HepG2	liver:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
36	CTCF	chr2:133304686-133304941	A549	lung:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
37	CTCF	chr2:133304520-133304636	GM19239	blood:	n/a	n/a
38	CTCF	chr2:133304760-133304910	GM12872	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
39	CTCF	chr2:133304760-133304910	GM12865	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
40	CTCF	chr2:133304760-133304910	GM12874	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
41	CTCF	chr2:133304523-133304980	GM13977	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
42	CTCF	chr2:133304742-133304973	ProgFib	skin:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
43	CTCF	chr2:133304800-133304950	NHDF-neo	bronchial:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
44	CTCF	chr2:133304649-133304990	H1-hESC	embryonic stem cell:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
45	CTCF	chr2:133304780-133304930	HEEpiC	esophagus:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
46	CTCF	chr2:133304780-133304930	GM12873	blood:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
47	CTCF	chr2:133304420-133304570	HEK293	kidney:	n/a	n/a
48	CTCF	chr2:133304800-133304950	HCPEpiC	choroid plexus:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
49	CTCF	chr2:133304708-133304991	Lung_OC	lung:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866
50	CTCF	chr2:133304804-133304927	MCF-7	breast:	n/a	chr2:133304854-133304872 chr2:133304856-133304877 chr2:133304857-133304870 chr2:133304857-133304866

No.	Distal block	Cell Line	Cell type
1	chr2:133304031..133305145-chr2:133928594..133929580,6	MCF-7	breast:
2	chr2:133304762..133308062-chr2:133425978..133429369,3	MCF-7	breast:
3	chr2:133304353..133304857-chr2:134601593..134602264,2	MCF-7	breast:
4	chr2:133308087..133308889-chr2:133339718..133340292,2	MCF-7	breast:
5	chr2:133274709..133277168-chr2:133277775..133280190,2	K562	blood:
6	chr2:133304640..133305382-chr2:133928983..133929651,2	MCF-7	breast:
7	chr2:133304368..133305326-chr2:134601553..134602523,5	K562	blood:
8	chr2:133304876..133306446-chr2:133426520..133428307,2	MCF-7	breast:
9	chr2:133304259..133305229-chr2:133647133..133647703,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2orf27A-10	chr2:133281190-133281509	NONHSAT074537

Variant related genes	Relation type
ENSG00000221142	TF binding region
RN7SKP103	TF binding region
ENSG00000150551	chromatin interactions

Extended variants
information (count: 1295 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1295 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4395295	chr2:133277683-133277684	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564496427	chr2:133277684-133277685	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs2315597	chr2:133277704-133277705	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs547277264	chr2:133277732-133277733	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs2315598	chr2:133277754-133277755	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs529661972	chr2:133277759-133277760	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs536088785	chr2:133277779-133277780	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs535646785	chr2:133277801-133277802	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs550285569	chr2:133277809-133277810	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs568870968	chr2:133277822-133277823	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs539128830	chr2:133277827-133277828	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs557854304	chr2:133277829-133277830	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs566282593	chr2:133277836-133277837	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs555566947	chr2:133277951-133277952	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs572430650	chr2:133278004-133278005	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs2872962	chr2:133278005-133278006	Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs555180047	chr2:133278066-133278067	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs573595282	chr2:133278087-133278088	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs182536125	chr2:133278101-133278102	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs557061549	chr2:133278172-133278173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575618003	chr2:133278193-133278194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564443386	chr2:133278261-133278262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545931462	chr2:133278281-133278282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs28460430	chr2:133278364-133278365	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs138551012	chr2:133278366-133278367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368648244	chr2:133278370-133278371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562298410	chr2:133278376-133278377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529599191	chr2:133278397-133278398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543419975	chr2:133278420-133278421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551274340	chr2:133278451-133278452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372552784	chr2:133278463-133278464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7571728	chr2:133278478-133278479	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs532942375	chr2:133278517-133278518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10191510	chr2:133278540-133278541	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs116403673	chr2:133278631-133278632	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs533686509	chr2:133278634-133278635	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs115274802	chr2:133278649-133278650	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs567156925	chr2:133278650-133278651	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs537714324	chr2:133278657-133278658	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs556426888	chr2:133278663-133278664	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs575510420	chr2:133278681-133278682	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs4954338	chr2:133278691-133278692	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs142742108	chr2:133278693-133278694	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs541121072	chr2:133278695-133278696	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs116259797	chr2:133278716-133278717	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs200991430	chr2:133278737-133278738	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs540767218	chr2:133278781-133278782	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs562232079	chr2:133278794-133278795	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs559863486	chr2:133278884-133278885	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs574200484	chr2:133278885-133278886	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	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
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133262000-133280400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:133268200-133282800	Weak transcription	Fetal Intestine Small	intestine
3	chr2:133269400-133278400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:133272800-133278600	Weak transcription	Fetal Heart	heart
5	chr2:133274400-133280200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:133274400-133283200	Weak transcription	Pancreas	Pancrea
7	chr2:133275400-133278600	Weak transcription	NHEK	skin
8	chr2:133277600-133277800	Enhancers	Brain Germinal Matrix	brain
9	chr2:133278000-133279000	Weak transcription	Brain Germinal Matrix	brain
10	chr2:133278400-133280800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:133278600-133278800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr2:133278600-133279200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr2:133278600-133279200	Enhancers	Fetal Heart	heart
14	chr2:133278600-133279200	Enhancers	NHEK	skin
15	chr2:133278600-133279400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr2:133278600-133279600	Enhancers	HMEC	breast
17	chr2:133278600-133280600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:133278600-133281000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr2:133278800-133279400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr2:133278800-133280400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:133279000-133279200	Enhancers	Fetal Brain Female	brain
22	chr2:133279000-133280800	Enhancers	Brain Germinal Matrix	brain
23	chr2:133279000-133282600	Enhancers	Fetal Brain Male	brain
24	chr2:133279200-133280200	Weak transcription	Fetal Brain Female	brain
25	chr2:133279200-133280200	Weak transcription	NHEK	skin
26	chr2:133279200-133281600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr2:133279200-133283000	Weak transcription	Fetal Heart	heart
28	chr2:133279400-133280400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr2:133279600-133280000	Weak transcription	HMEC	breast
30	chr2:133279800-133281200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr2:133280000-133280800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr2:133280000-133280800	Enhancers	HMEC	breast
33	chr2:133280200-133280600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr2:133280200-133280600	Enhancers	NHEK	skin
35	chr2:133280200-133281000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr2:133280200-133281400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr2:133280200-133281400	Enhancers	Fetal Brain Female	brain
38	chr2:133280400-133280600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr2:133280400-133280800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr2:133280400-133281200	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr2:133280400-133281200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr2:133280800-133281200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:133281200-133281400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr2:133281200-133281800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr2:133281400-133296400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr2:133281800-133282000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr2:133282000-133284600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr2:133282800-133284800	ZNF genes & repeats	Fetal Intestine Small	intestine
49	chr2:133283000-133283800	Enhancers	Fetal Heart	heart
50	chr2:133283200-133283400	Genic enhancers	Pancreas	Pancrea

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