Variant report

Variant	esv3499566
Chromosome Location	chr4:49176864-49250831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1857)
CpG islands
(count:244)
Chromatin interactive
region (count:0)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1857 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:49219672-49219782	K562	blood:	n/a	n/a
2	BATF	chr4:49203192-49203619	GM12878	blood:	n/a	n/a
3	BATF	chr4:49198280-49198474	GM12878	blood:	n/a	n/a
4	BATF	chr4:49183824-49184999	GM12878	blood:	n/a	n/a
5	BATF	chr4:49198789-49199210	GM12878	blood:	n/a	n/a
6	BATF	chr4:49211509-49211776	GM12878	blood:	n/a	n/a
7	BATF	chr4:49202607-49202811	GM12878	blood:	n/a	n/a
8	BATF	chr4:49187844-49188518	GM12878	blood:	n/a	n/a
9	BATF	chr4:49240544-49240716	GM12878	blood:	n/a	n/a
10	BATF	chr4:49200976-49201419	GM12878	blood:	n/a	n/a
11	BATF	chr4:49194228-49194538	GM12878	blood:	n/a	n/a
12	BATF	chr4:49182870-49183109	GM12878	blood:	n/a	n/a
13	BATF	chr4:49250375-49250617	GM12878	blood:	n/a	n/a
14	BATF	chr4:49187322-49187755	GM12878	blood:	n/a	n/a
15	BATF	chr4:49196142-49196389	GM12878	blood:	n/a	n/a
16	BATF	chr4:49226213-49226403	GM12878	blood:	n/a	n/a
17	BATF	chr4:49200082-49200414	GM12878	blood:	n/a	n/a
18	BATF	chr4:49204293-49204573	GM12878	blood:	n/a	n/a
19	BATF	chr4:49186781-49187365	GM12878	blood:	n/a	n/a
20	BATF	chr4:49249355-49249684	GM12878	blood:	n/a	n/a
21	BATF	chr4:49193638-49193955	GM12878	blood:	n/a	n/a
22	BATF	chr4:49203975-49204281	GM12878	blood:	n/a	n/a
23	BATF	chr4:49204025-49204544	GM12878	blood:	n/a	n/a
24	BATF	chr4:49185256-49185588	GM12878	blood:	n/a	n/a
25	BATF	chr4:49197009-49197431	GM12878	blood:	n/a	n/a
26	BATF	chr4:49182780-49183741	GM12878	blood:	n/a	n/a
27	BATF	chr4:49193971-49194254	GM12878	blood:	n/a	n/a
28	BATF	chr4:49180996-49181347	GM12878	blood:	n/a	n/a
29	BATF	chr4:49196148-49196381	GM12878	blood:	n/a	n/a
30	BATF	chr4:49186720-49187236	GM12878	blood:	n/a	n/a
31	BATF	chr4:49195065-49195673	GM12878	blood:	n/a	n/a
32	BATF	chr4:49184309-49184879	GM12878	blood:	n/a	n/a
33	BATF	chr4:49248328-49248546	GM12878	blood:	n/a	n/a
34	BATF	chr4:49181450-49181651	GM12878	blood:	n/a	n/a
35	BATF	chr4:49200948-49201240	GM12878	blood:	n/a	n/a
36	BATF	chr4:49196588-49196834	GM12878	blood:	n/a	n/a
37	BATF	chr4:49247937-49248234	GM12878	blood:	n/a	n/a
38	BATF	chr4:49181930-49182132	GM12878	blood:	n/a	n/a
39	BATF	chr4:49195151-49195336	GM12878	blood:	n/a	n/a
40	BATF	chr4:49203258-49203635	GM12878	blood:	n/a	n/a
41	BATF	chr4:49199682-49200057	GM12878	blood:	n/a	n/a
42	BATF	chr4:49197708-49198269	GM12878	blood:	n/a	n/a
43	BATF	chr4:49200625-49200836	GM12878	blood:	n/a	n/a
44	BATF	chr4:49201857-49202145	GM12878	blood:	n/a	n/a
45	BATF	chr4:49187369-49187639	GM12878	blood:	n/a	n/a
46	BATF	chr4:49183830-49184242	GM12878	blood:	n/a	n/a
47	BATF	chr4:49198779-49199325	GM12878	blood:	n/a	n/a
48	BATF	chr4:49248767-49249200	GM12878	blood:	n/a	n/a
49	BATF	chr4:49181376-49181626	GM12878	blood:	n/a	n/a
50	BATF	chr4:49196524-49196831	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:49237109-49237159	AG04449	skin:	fetal
2	chr4:49204696-49204746	NH-A	brain:	n/a
3	chr4:49204696-49204746	IMR90	lung:	fetal
4	chr4:49237109-49237159	Jurkat	blood:	n/a
5	chr4:49237497-49237547	NH-A	brain:	n/a
6	chr4:49237109-49237159	SKMC	muscle:	n/a
7	chr4:49204696-49204746	K562	blood:	n/a
8	chr4:49204696-49204746	NHDF-neo	bronchial:	n/a
9	chr4:49237497-49237547	HUVEC	blood vessel:	n/a
10	chr4:49236405-49236455	K562	blood:	n/a
11	chr4:49204696-49204746	HCM	heart:	n/a
12	chr4:49237109-49237159	HCPEpiC	choroid plexus:	n/a
13	chr4:49236405-49236455	SK-N-SH_RA	brain:	n/a
14	chr4:49204696-49204746	RPTEC	kidney:	n/a
15	chr4:49204696-49204746	AG04449	skin:	fetal
16	chr4:49237497-49237547	NHBE	bronchial:	n/a
17	chr4:49237497-49237547	GM12878	blood:	n/a
18	chr4:49237109-49237159	HPAEpiC	pulmonary alveolar:	n/a
19	chr4:49237497-49237547	CMK	blood:	n/a
20	chr4:49236405-49236455	A549	lung:	n/a
21	chr4:49237109-49237159	CMK	blood:	n/a
22	chr4:49237109-49237159	SAEC	small airway:	n/a
23	chr4:49204696-49204746	H1-hESC	embryonic stem cell:	embryo
24	chr4:49236405-49236455	NH-A	brain:	n/a
25	chr4:49236405-49236455	SK-N-SH	brain:	n/a
26	chr4:49236405-49236455	CMK	blood:	n/a
27	chr4:49204696-49204746	HIPEpiC	eye:	n/a
28	chr4:49204696-49204746	A549	lung:	n/a
29	chr4:49204696-49204746	HepG2	liver:	n/a
30	chr4:49204696-49204746	U87	brain:	n/a
31	chr4:49204696-49204746	T-47D	breast:	n/a
32	chr4:49237109-49237159	Hela-S3	cervix:	n/a
33	chr4:49204696-49204746	HCPEpiC	choroid plexus:	n/a
34	chr4:49237497-49237547	HIPEpiC	eye:	n/a
35	chr4:49236405-49236455	ProgFib	skin:	n/a
36	chr4:49237109-49237159	HCF	heart:	n/a
37	chr4:49237497-49237547	ECC-1	luminal epithelium:	n/a
38	chr4:49237109-49237159	SK-N-SH	brain:	n/a
39	chr4:49204696-49204746	GM12892	blood:	n/a
40	chr4:49237497-49237547	HepG2	liver:	n/a
41	chr4:49236405-49236455	HUVEC	blood vessel:	n/a
42	chr4:49204696-49204746	PANC-1	pancreas:	n/a
43	chr4:49236405-49236455	LNCaP	prostate:	n/a
44	chr4:49236405-49236455	SKMC	muscle:	n/a
45	chr4:49236405-49236455	ovcar-3	ovarian:	n/a
46	chr4:49237497-49237547	T-47D	breast:	n/a
47	chr4:49237497-49237547	Hepatocyte	liver:	n/a
48	chr4:49237109-49237159	HUVEC	blood vessel:	n/a
49	chr4:49204696-49204746	HAEpiC	amniotic membrane:	n/a
50	chr4:49236405-49236455	MCF-7	breast:	n/a

No data

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCIAD2-6	chr4:49221527-49221803	NONHSAT096315
2	lnc-CWH43-4	chr4:49248038-49248555	NONHSAT096323
3	lnc-OCIAD2-9	chr4:49246290-49246387	NONHSAT096322
4	lnc-OCIAD2-7	chr4:49231590-49233301	NONHSAT096320
5	lnc-OCIAD2-9	chr4:49239116-49239167	NONHSAT096322
6	lnc-OCIAD2-9	chr4:49244726-49244948	NONHSAT096322
7	lnc-OCIAD2-9	chr4:49241263-49241308	NONHSAT096322
8	lnc-OCIAD2-9	chr4:49239669-49239711	NONHSAT096322
9	lnc-OCIAD2-5	chr4:49214268-49214641	NONHSAT096314
10	lnc-CWH43-5	chr4:49248783-49248932	NONHSAT096324
11	lnc-CWH43-5	chr4:49248618-49248710	NONHSAT096324
12	lnc-OCIAD2-9	chr4:49240040-49240093	NONHSAT096322

No data

Variant related genes	Relation type
ENSG00000249079	TF binding region
ENSG00000221747	TF binding region
ENSG00000266337	TF binding region
ENSG00000248946	TF binding region
ENSG00000249828	TF binding region
ENSG00000222437	TF binding region
ENSG00000237961	TF binding region
ENSG00000268736	TF binding region
SNX18P23	TF binding region
ENSG00000221415	TF binding region
ENSG00000249079	CpG island
ENSG00000221747	CpG island
ENSG00000266337	CpG island
ENSG00000248946	CpG island
ENSG00000249828	CpG island
ENSG00000222437	CpG island
ENSG00000237961	CpG island
ENSG00000268736	CpG island
SNX18P23	CpG island
ENSG00000221415	CpG island

Extended variants
information (count: 4449 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:4449 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6829391	chr4:49177014-49177015	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191589263	chr4:49177015-49177016	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577744958	chr4:49177033-49177034	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs77155106	chr4:49177038-49177039	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78121442	chr4:49177044-49177045	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78277237	chr4:49177053-49177054	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142340969	chr4:49177058-49177059	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77516531	chr4:49177062-49177063	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs9685850	chr4:49177081-49177082	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79009032	chr4:49177088-49177089	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75766940	chr4:49177097-49177098	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76261298	chr4:49177107-49177108	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs6852869	chr4:49177114-49177115	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545138599	chr4:49177116-49177117	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs9685851	chr4:49177119-49177120	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs75413714	chr4:49177121-49177122	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6447719	chr4:49177131-49177132	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs76262350	chr4:49177143-49177144	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530533225	chr4:49177149-49177150	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79508358	chr4:49177151-49177152	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78970190	chr4:49177157-49177158	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs76743721	chr4:49177170-49177171	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149878632	chr4:49177182-49177183	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377059065	chr4:49177191-49177192	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2931976	chr4:49177196-49177197	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555469861	chr4:49177201-49177202	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs62297345	chr4:49177203-49177204	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs6851606	chr4:49177215-49177216	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2931975	chr4:49177221-49177222	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566279556	chr4:49177229-49177230	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373774660	chr4:49177232-49177233	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200459287	chr4:49177240-49177241	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539617991	chr4:49177241-49177242	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551464552	chr4:49177242-49177243	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187774273	chr4:49177247-49177248	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6829579	chr4:49177248-49177249	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537138939	chr4:49177249-49177250	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2450959	chr4:49177250-49177251	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369096402	chr4:49177262-49177263	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183765706	chr4:49177266-49177267	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374913371	chr4:49177272-49177273	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555386992	chr4:49177280-49177281	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573928160	chr4:49177281-49177282	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534950017	chr4:49177284-49177285	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367615012	chr4:49177302-49177303	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552956128	chr4:49177319-49177320	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs201634812	chr4:49177323-49177324	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2450958	chr4:49177324-49177325	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200270907	chr4:49177330-49177331	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577787476	chr4:49177347-49177348	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	16272173	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:49177000-49177400	Enhancers	K562	blood
2	chr4:49177000-49177800	ZNF genes & repeats	Adipose Nuclei	Adipose
3	chr4:49177400-49177800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:49177400-49177800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:49177400-49177800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:49177400-49177800	Flanking Active TSS	K562	blood
7	chr4:49177800-49179800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:49177800-49180000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:49177800-49184000	Weak transcription	K562	blood
10	chr4:49179800-49180400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr4:49180000-49180400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr4:49180000-49181200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:49180000-49181200	ZNF genes & repeats	Spleen	Spleen
14	chr4:49181200-49183600	Weak transcription	Spleen	Spleen
15	chr4:49184000-49184200	Enhancers	K562	blood
16	chr4:49199000-49200400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:49199800-49200400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
18	chr4:49212600-49213600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:49212600-49240600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:49213400-49217200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr4:49213400-49224600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:49213600-49214000	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:49213600-49214200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:49213600-49214200	ZNF genes & repeats	Spleen	Spleen
25	chr4:49213600-49217200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
26	chr4:49213800-49214000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr4:49214000-49214200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:49214200-49215200	Weak transcription	Spleen	Spleen
29	chr4:49214200-49219200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:49215200-49216800	ZNF genes & repeats	Spleen	Spleen
31	chr4:49215400-49217400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:49215800-49217000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:49216000-49216600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
34	chr4:49216000-49217000	ZNF genes & repeats	Gastric	stomach
35	chr4:49216000-49217000	Enhancers	Right Ventricle	heart
36	chr4:49216200-49216400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr4:49216200-49217600	Enhancers	K562	blood
38	chr4:49217600-49219200	Weak transcription	K562	blood
39	chr4:49219200-49220000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:49219200-49220400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:49219200-49220400	Enhancers	K562	blood
42	chr4:49219600-49220200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
43	chr4:49220000-49236400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:49220800-49222000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:49220800-49224400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
46	chr4:49221000-49222200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr4:49221000-49223800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:49221000-49224000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
49	chr4:49221000-49225200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr4:49221200-49221800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links