Variant report

Variant	nsv581928
Chromosome Location	chr2:52572167-52656594
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	CEBPB	chr2:52616319-52616570	HepG2	liver:	n/a	chr2:52616446-52616457 chr2:52616447-52616458 chr2:52616446-52616459
2	CEBPB	chr2:52650929-52651105	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr2:52623783-52624296	HepG2	liver:	n/a	chr2:52624106-52624117
4	CEBPB	chr2:52650239-52651116	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr2:52656477-52657495	Hela-S3	cervix:	n/a	chr2:52657151-52657160 chr2:52657086-52657099 chr2:52657149-52657162 chr2:52657151-52657162 chr2:52657151-52657160 chr2:52657149-52657162 chr2:52657151-52657160 chr2:52657434-52657447 chr2:52657151-52657160 chr2:52657149-52657160
6	CHD1	chr2:52640945-52640985	GM12878	blood:	n/a	n/a
7	CHD2	chr2:52638167-52638367	K562	blood:	n/a	n/a
8	CTCF	chr2:52643530-52643848	GM12878	blood:	n/a	chr2:52643676-52643694
9	CTCF	chr2:52643640-52643790	A549	lung:	n/a	chr2:52643676-52643694
10	CTCF	chr2:52643629-52643688	ProgFib	skin:	n/a	n/a
11	CTCF	chr2:52643580-52643730	HPF	lung:	n/a	chr2:52643676-52643694
12	CTCF	chr2:52643480-52643630	HEEpiC	esophagus:	n/a	n/a
13	CTCF	chr2:52643600-52643750	GM12878	blood:	n/a	chr2:52643676-52643694
14	CTCF	chr2:52636480-52636630	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr2:52643600-52643750	HEK293	kidney:	n/a	chr2:52643676-52643694
16	CTCF	chr2:52643580-52643730	HCPEpiC	choroid plexus:	n/a	chr2:52643676-52643694
17	CTCF	chr2:52643580-52643730	AG04450	lung:	n/a	chr2:52643676-52643694
18	CTCF	chr2:52643520-52643670	BE2_C	brain:	n/a	n/a
19	CTCF	chr2:52643640-52643790	Caco-2	colon:	n/a	chr2:52643676-52643694
20	CTCF	chr2:52643433-52643911	HCT-116	colon:	n/a	chr2:52643676-52643694
21	CTCF	chr2:52636534-52636641	Gliobla	brain:	n/a	n/a
22	CTCF	chr2:52643577-52643775	HepG2	liver:	n/a	chr2:52643676-52643694
23	CTCF	chr2:52643600-52643750	AG04449	skin:	n/a	chr2:52643676-52643694
24	CTCF	chr2:52655414-52655693	H1-hESC	embryonic stem cell:	n/a	chr2:52655506-52655519 chr2:52655597-52655604
25	CTCF	chr2:52643516-52643853	IMR90	lung:	n/a	chr2:52643676-52643694
26	CTCF	chr2:52643580-52643730	GM12872	blood:	n/a	chr2:52643676-52643694
27	CTCF	chr2:52643568-52643765	Gliobla	brain:	n/a	chr2:52643676-52643694
28	CTCF	chr2:52613860-52614010	GM12875	blood:	n/a	n/a
29	CTCF	chr2:52643600-52643750	SAEC	small airway:	n/a	chr2:52643676-52643694
30	CTCF	chr2:52643580-52643730	HMEC	breast:	n/a	chr2:52643676-52643694
31	CTCF	chr2:52636540-52636690	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr2:52643668-52643687	MCF-7	breast:	n/a	n/a
33	CTCF	chr2:52643500-52643650	HAc	cerebellar:	n/a	n/a
34	CTCF	chr2:52643520-52643670	HRE	kidney:	n/a	n/a
35	CTCF	chr2:52643760-52643910	NHEK	skin:	n/a	n/a
36	CTCF	chr2:52655480-52655630	HEK293	kidney:	n/a	chr2:52655506-52655519 chr2:52655597-52655604
37	CTCF	chr2:52643600-52643750	Caco-2	colon:	n/a	chr2:52643676-52643694
38	CTCF	chr2:52643666-52643739	GM13977	blood:	n/a	chr2:52643676-52643694
39	CTCF	chr2:52643380-52643530	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr2:52643580-52643730	HCFaa	heart:	n/a	chr2:52643676-52643694
41	CTCF	chr2:52643640-52643790	HA-sp	spinal cord:	n/a	chr2:52643676-52643694
42	CTCF	chr2:52655380-52655530	A549	lung:	n/a	chr2:52655506-52655519
43	CTCF	chr2:52643540-52643690	NHEK	skin:	n/a	n/a
44	CTCF	chr2:52636480-52636630	HEK293	kidney:	n/a	n/a
45	CTCF	chr2:52585340-52585400	GM20000	blood:	n/a	n/a
46	CTCF	chr2:52643460-52643610	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:52643580-52643730	SAEC	small airway:	n/a	chr2:52643676-52643694
48	CTCF	chr2:52636448-52636746	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr2:52594040-52594190	GM12869	blood:	n/a	n/a
50	CTCF	chr2:52643580-52643830	HMEC	breast:	n/a	chr2:52643676-52643694

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52614831-52614881	HCM	heart:	n/a
2	chr2:52614831-52614881	SK-N-SH_RA	brain:	n/a
3	chr2:52614831-52614881	ovcar-3	ovarian:	n/a
4	chr2:52614831-52614881	PrEC	prostate:	n/a
5	chr2:52614831-52614881	AG04449	skin:	fetal
6	chr2:52614831-52614881	HUVEC	blood vessel:	n/a
7	chr2:52614831-52614881	NHBE	bronchial:	n/a
8	chr2:52614831-52614881	HIPEpiC	eye:	n/a
9	chr2:52614831-52614881	GM19239	blood:	n/a
10	chr2:52614831-52614881	NT2-D1	testis:	n/a
11	chr2:52614831-52614881	HEEpiC	esophagus:	n/a
12	chr2:52614831-52614881	ProgFib	skin:	n/a
13	chr2:52614831-52614881	H1-hESC	embryonic stem cell:	embryo
14	chr2:52614831-52614881	SK-N-SH	brain:	n/a
15	chr2:52614831-52614881	LNCaP	prostate:	n/a
16	chr2:52614831-52614881	BE2_C	brain:	n/a
17	chr2:52614831-52614881	HCF	heart:	n/a
18	chr2:52614831-52614881	HAEpiC	amniotic membrane:	n/a
19	chr2:52614831-52614881	Hepatocyte	liver:	n/a
20	chr2:52614831-52614881	HRE	kidney:	n/a
21	chr2:52614831-52614881	NB4	blood:	n/a
22	chr2:52614831-52614881	AG04450	lung:	fetal
23	chr2:52614831-52614881	AG09319	gingival:	n/a
24	chr2:52614831-52614881	AG10803	skin:	n/a
25	chr2:52614831-52614881	T-47D	breast:	n/a
26	chr2:52614831-52614881	AG09309	skin:	n/a
27	chr2:52614831-52614881	U87	brain:	n/a
28	chr2:52614831-52614881	IMR90	lung:	fetal
29	chr2:52614831-52614881	HRCEpiC	kidney:	n/a
30	chr2:52614831-52614881	HRPEpiC	eye:	n/a
31	chr2:52614831-52614881	SAEC	small airway:	n/a
32	chr2:52614831-52614881	PFSK-1	brain:	n/a
33	chr2:52614831-52614881	HCPEpiC	choroid plexus:	n/a
34	chr2:52614831-52614881	HMEC	breast:	n/a
35	chr2:52614831-52614881	MCF-7	breast:	n/a
36	chr2:52614831-52614881	PANC-1	pancreas:	n/a
37	chr2:52614831-52614881	SKMC	muscle:	n/a
38	chr2:52614831-52614881	GM06990	blood:	n/a
39	chr2:52614831-52614881	HNPCEpiC	eye:	n/a
40	chr2:52614831-52614881	Jurkat	blood:	n/a
41	chr2:52614831-52614881	SK-N-MC	brain:	n/a
42	chr2:52614831-52614881	CMK	blood:	n/a
43	chr2:52614831-52614881	K562	blood:	n/a
44	chr2:52614831-52614881	GM12892	blood:	n/a
45	chr2:52614831-52614881	HEK293	kidney:	embryo
46	chr2:52614831-52614881	NH-A	brain:	n/a
47	chr2:52614831-52614881	GM12891	blood:	n/a
48	chr2:52614831-52614881	HL-60	blood:	n/a
49	chr2:52614831-52614881	NHDF-neo	bronchial:	n/a
50	chr2:52614831-52614881	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:52618576..52620644-chr2:52620820..52623618,2	MCF-7	breast:
2	chr2:52618576..52620644-chr2:52620820..52623618,2	MCF-7	breast:
3	chr2:52644535..52645157-chr2:52839947..52840842,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-4	chr2:52580012-52580100	ENSG00000231918.1
2	lnc-CHAC2-4	chr2:52576463-52578424	ENSG00000231918.1
3	lnc-CHAC2-3	chr2:52600256-52600309	XLOC_001468
4	lnc-ASB3-11	chr2:52576407-52576478	NONHSAT070669
5	lnc-CHAC2-4	chr2:52634116-52635055	ENSG00000231918.1
6	lnc-ASB3-11	chr2:52575330-52575504	NONHSAT070669
7	lnc-ASB3-11	chr2:52581186-52581394	NONHSAT070669
8	lnc-ASB3-11	chr2:52579245-52579427	NONHSAT070669
9	lnc-CHAC2-3	chr2:52616601-52617150	XLOC_001468

Variant related genes	Relation type
ENSG00000225444	TF binding region
ENSG00000225444	CpG island

Extended variants
information (count: 3523 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3523 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2081375	chr2:52572167-52572168	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74537034	chr2:52572219-52572220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563150042	chr2:52572272-52572273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78065908	chr2:52572316-52572317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs373337928	chr2:52572353-52572354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376760732	chr2:52572356-52572357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77794071	chr2:52572363-52572364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs67787703	chr2:52572364-52572365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72332765	chr2:52572371-52572372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs61698584	chr2:52572388-52572389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201624144	chr2:52572389-52572390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs199951378	chr2:52572391-52572392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73931304	chr2:52572400-52572401	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs531202583	chr2:52572426-52572427	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551320409	chr2:52572439-52572440	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563231622	chr2:52572449-52572450	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532155169	chr2:52572463-52572464	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186540334	chr2:52572468-52572469	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565828165	chr2:52572469-52572470	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs151044416	chr2:52572472-52572473	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79000166	chr2:52572562-52572563	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532164525	chr2:52572582-52572583	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35779064	chr2:52572595-52572596	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2552337	chr2:52572629-52572630	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs76811159	chr2:52572640-52572641	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191368204	chr2:52572642-52572643	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185380767	chr2:52572688-52572689	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553045554	chr2:52572745-52572746	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573323898	chr2:52572768-52572769	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369244356	chr2:52572770-52572771	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189096224	chr2:52572775-52572776	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562282925	chr2:52572785-52572786	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2552338	chr2:52572806-52572807	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs193143145	chr2:52572829-52572830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185279969	chr2:52572838-52572839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189189466	chr2:52572852-52572853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139684676	chr2:52572860-52572861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs116212588	chr2:52572862-52572863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528153695	chr2:52572908-52572909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548002264	chr2:52572965-52572966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149809448	chr2:52572970-52572971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs17042782	chr2:52572987-52572988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550448267	chr2:52573002-52573003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115691177	chr2:52573009-52573010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539423983	chr2:52573011-52573012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181211409	chr2:52573061-52573062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566775729	chr2:52573062-52573063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535898553	chr2:52573063-52573064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145759912	chr2:52573095-52573096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569056083	chr2:52573096-52573097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52564400-52572400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:52565000-52577800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr2:52567400-52583600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:52569800-52573000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr2:52569800-52573400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr2:52571200-52579800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:52571400-52572200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr2:52571400-52572400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr2:52571400-52572400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:52571400-52572400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr2:52571400-52572400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr2:52571400-52572600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr2:52572000-52573000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr2:52572000-52573000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr2:52572000-52573200	Enhancers	H9 Cell Line	embryonic stem cell
16	chr2:52572200-52572600	Enhancers	Fetal Brain Male	brain
17	chr2:52572200-52573400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr2:52572400-52572600	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr2:52572400-52573000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr2:52572400-52573200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr2:52572400-52573200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr2:52572400-52573200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr2:52572400-52573400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr2:52572600-52572800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr2:52572600-52573200	Enhancers	H1 Cell Line	embryonic stem cell
26	chr2:52572800-52573000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr2:52573000-52573600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr2:52573000-52579800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr2:52573200-52583800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr2:52573400-52574400	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr2:52573600-52578800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:52574400-52585400	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr2:52579800-52580200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
34	chr2:52579800-52581600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr2:52580200-52585800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr2:52581600-52584000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:52583600-52584000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr2:52583600-52584000	Enhancers	Colon Smooth Muscle	Colon
39	chr2:52583600-52584200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr2:52583800-52584000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr2:52583800-52584200	Enhancers	Fetal Lung	lung
42	chr2:52585400-52587800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr2:52585800-52586800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
44	chr2:52586200-52586600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr2:52586600-52590600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr2:52587800-52591000	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr2:52588600-52589800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr2:52589800-52592000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:52591000-52591600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
50	chr2:52591200-52591400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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