Variant report

Variant	esv1797464
Chromosome Location	chr16:46820464-46857454
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	chr16:46823112-46823219	HepG2	liver:	n/a	n/a
2	ATF2	chr16:46821651-46822239	GM12878	blood:	n/a	n/a
3	ATF2	chr16:46855981-46856766	GM12878	blood:	n/a	n/a
4	ATF2	chr16:46821736-46822190	GM12878	blood:	n/a	n/a
5	ATF2	chr16:46856044-46856624	GM12878	blood:	n/a	n/a
6	BACH1	chr16:46837364-46837547	K562	blood:	n/a	n/a
7	BACH1	chr16:46823539-46823617	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr16:46837370-46837615	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr16:46847070-46847406	GM12878	blood:	n/a	chr16:46847248-46847259
10	BATF	chr16:46856088-46856521	GM12878	blood:	n/a	n/a
11	BATF	chr16:46856078-46856518	GM12878	blood:	n/a	n/a
12	BCL11A	chr16:46856181-46856530	GM12878	blood:	n/a	chr16:46856476-46856485
13	BCL3	chr16:46823823-46824359	GM12878	blood:	n/a	chr16:46824206-46824215 chr16:46824033-46824046
14	BCL3	chr16:46856188-46856585	GM12878	blood:	n/a	chr16:46856476-46856485
15	BCLAF1	chr16:46823337-46823801	GM12878	blood:	n/a	n/a
16	BCLAF1	chr16:46855938-46856575	GM12878	blood:	n/a	chr16:46856476-46856485
17	BCLAF1	chr16:46823890-46824608	GM12878	blood:	n/a	chr16:46824206-46824215 chr16:46824033-46824046
18	BCLAF1	chr16:46855988-46856728	GM12878	blood:	n/a	chr16:46856476-46856485
19	BHLHE40	chr16:46823952-46824337	GM12878	blood:	n/a	n/a
20	BHLHE40	chr16:46824026-46824172	K562	blood:	n/a	n/a
21	BRCA1	chr16:46856315-46856327	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr16:46823860-46824112	GM12878	blood:	n/a	n/a
23	BRCA1	chr16:46823854-46824119	HepG2	liver:	n/a	n/a
24	BRCA1	chr16:46823802-46824117	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr16:46823810-46824113	Hela-S3	cervix:	n/a	n/a
26	CCNT2	chr16:46823844-46824237	K562	blood:	n/a	n/a
27	CEBPB	chr16:46822199-46822268	HepG2	liver:	n/a	chr16:46822245-46822256
28	CEBPB	chr16:46843922-46844068	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr16:46821735-46821791	IMR90	lung:	n/a	n/a
30	CEBPB	chr16:46821709-46821870	HepG2	liver:	n/a	n/a
31	CEBPB	chr16:46821725-46821899	K562	blood:	n/a	n/a
32	CEBPB	chr16:46856255-46856496	Hela-S3	cervix:	n/a	n/a
33	CEBPD	chr16:46823819-46824302	HepG2	liver:	n/a	n/a
34	CHD2	chr16:46823747-46824244	HepG2	liver:	n/a	n/a
35	CHD2	chr16:46823745-46824217	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr16:46823753-46824219	K562	blood:	n/a	n/a
37	CHD2	chr16:46823611-46824203	GM12878	blood:	n/a	n/a
38	CHD2	chr16:46823761-46824247	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr16:46835460-46835610	GM12878	blood:	n/a	chr16:46835544-46835565 chr16:46835549-46835567 chr16:46835550-46835566 chr16:46835551-46835564
40	CTCF	chr16:46835460-46835610	HL-60	blood:	n/a	chr16:46835544-46835565 chr16:46835549-46835567 chr16:46835550-46835566 chr16:46835551-46835564
41	CTCF	chr16:46835301-46835817	HCT-116	colon:	n/a	chr16:46835544-46835565 chr16:46835549-46835567 chr16:46835550-46835566 chr16:46835551-46835564
42	CTCF	chr16:46835460-46835610	GM12865	blood:	n/a	chr16:46835544-46835565 chr16:46835549-46835567 chr16:46835550-46835566 chr16:46835551-46835564
43	CTCF	chr16:46827400-46827550	HepG2	liver:	n/a	n/a
44	CTCF	chr16:46824620-46824770	BE2_C	brain:	n/a	n/a
45	CTCF	chr16:46835480-46835630	HCM	heart:	n/a	chr16:46835544-46835565 chr16:46835549-46835567 chr16:46835550-46835566 chr16:46835551-46835564
46	CTCF	chr16:46835480-46835630	NHLF	lung:	n/a	chr16:46835544-46835565 chr16:46835549-46835567 chr16:46835550-46835566 chr16:46835551-46835564
47	CTCF	chr16:46835440-46835590	GM06990	blood:	n/a	chr16:46835544-46835565 chr16:46835549-46835567 chr16:46835550-46835566 chr16:46835551-46835564
48	CTCF	chr16:46835480-46835630	HMF	breast:	n/a	chr16:46835544-46835565 chr16:46835549-46835567 chr16:46835550-46835566 chr16:46835551-46835564
49	CTCF	chr16:46835520-46835670	HRE	kidney:	n/a	chr16:46835544-46835565 chr16:46835549-46835567 chr16:46835550-46835566 chr16:46835551-46835564
50	CTCF	chr16:46835534-46835588	GM10248	blood:	n/a	chr16:46835544-46835565 chr16:46835549-46835567 chr16:46835550-46835566 chr16:46835551-46835564

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:46824055-46824105	T-47D	breast:	n/a
2	chr16:46824055-46824105	T-47D	breast:	n/a
3	chr16:46838434-46838484	GM12891	blood:	n/a
4	chr16:46823623-46823673	HPAEpiC	pulmonary alveolar:	n/a
5	chr16:46854830-46854880	AG04449	skin:	fetal
6	chr16:46854830-46854880	BE2_C	brain:	n/a
7	chr16:46821679-46821729	HepG2	liver:	n/a
8	chr16:46838434-46838484	U87	brain:	n/a
9	chr16:46836742-46836792	HAEpiC	amniotic membrane:	n/a
10	chr16:46826414-46826464	NHBE	bronchial:	n/a
11	chr16:46824519-46824569	T-47D	breast:	n/a
12	chr16:46826414-46826464	GM19239	blood:	n/a
13	chr16:46838434-46838484	HEEpiC	esophagus:	n/a
14	chr16:46836742-46836792	NHBE	bronchial:	n/a
15	chr16:46854830-46854880	SKMC	muscle:	n/a
16	chr16:46824143-46824193	U87	brain:	n/a
17	chr16:46824055-46824105	HPAEpiC	pulmonary alveolar:	n/a
18	chr16:46838434-46838484	HRPEpiC	eye:	n/a
19	chr16:46821679-46821729	HCM	heart:	n/a
20	chr16:46824519-46824569	Hepatocyte	liver:	n/a
21	chr16:46838434-46838484	HCF	heart:	n/a
22	chr16:46823623-46823673	K562	blood:	n/a
23	chr16:46824143-46824193	GM19239	blood:	n/a
24	chr16:46826414-46826464	HepG2	liver:	n/a
25	chr16:46824519-46824569	ovcar-3	ovarian:	n/a
26	chr16:46824143-46824193	SK-N-SH_RA	brain:	n/a
27	chr16:46823623-46823673	IMR90	lung:	fetal
28	chr16:46836742-46836792	PFSK-1	brain:	n/a
29	chr16:46838434-46838484	HUVEC	blood vessel:	n/a
30	chr16:46824519-46824569	U87	brain:	n/a
31	chr16:46824519-46824569	HCF	heart:	n/a
32	chr16:46823623-46823673	PFSK-1	brain:	n/a
33	chr16:46823623-46823673	PrEC	prostate:	n/a
34	chr16:46836742-46836792	AG09319	gingival:	n/a
35	chr16:46854830-46854880	HAEpiC	amniotic membrane:	n/a
36	chr16:46823623-46823673	BJ	skin:	n/a
37	chr16:46838434-46838484	PANC-1	pancreas:	n/a
38	chr16:46826414-46826464	Hela-S3	cervix:	n/a
39	chr16:46821679-46821729	HCPEpiC	choroid plexus:	n/a
40	chr16:46824519-46824569	HPAEpiC	pulmonary alveolar:	n/a
41	chr16:46823623-46823673	T-47D	breast:	n/a
42	chr16:46836742-46836792	HUVEC	blood vessel:	n/a
43	chr16:46838434-46838484	SK-N-SH	brain:	n/a
44	chr16:46826414-46826464	PFSK-1	brain:	n/a
45	chr16:46821679-46821729	SK-N-SH_RA	brain:	n/a
46	chr16:46836742-46836792	NT2-D1	testis:	n/a
47	chr16:46823935-46823985	HUVEC	blood vessel:	n/a
48	chr16:46854830-46854880	H1-hESC	embryonic stem cell:	embryo
49	chr16:46824143-46824193	HNPCEpiC	eye:	n/a
50	chr16:46826414-46826464	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr16:46854177..46856451-chr16:46859236..46861575,2	K562	blood:
2	chr16:46849547..46852828-chr16:46862623..46865184,3	K562	blood:
3	chr16:46831873..46834182-chr16:46837803..46840106,2	K562	blood:
4	chr16:46721038..46723850-chr16:46838933..46841050,2	K562	blood:
5	chr16:46823466..46824461-chr7:152456864..152457453,2	Hela-S3	cervix:
6	chr16:46852133..46853769-chr16:46855489..46857597,2	K562	blood:
7	chr16:46852902..46855463-chr16:46861590..46865288,6	K562	blood:
8	chr16:46722541..46725378-chr16:46836985..46838903,2	K562	blood:
9	chr16:46723658..46727681-chr16:46823795..46826359,3	K562	blood:
10	chr16:46852133..46853769-chr16:46855489..46857597,2	K562	blood:
11	chr16:46841434..46846391-chr16:46846846..46850783,4	K562	blood:
12	chr16:46721174..46723100-chr16:46834009..46836909,2	MCF-7	breast:
13	chr16:46722584..46725164-chr16:46820460..46823244,2	K562	blood:
14	chr16:46855816..46858578-chr16:46865585..46867919,2	MCF-7	breast:
15	chr16:46826593..46829284-chr16:46831194..46833933,2	K562	blood:
16	chr16:46808123..46810169-chr16:46845053..46846585,2	MCF-7	breast:
17	chr16:46826593..46829284-chr16:46831194..46833933,2	K562	blood:
18	chr16:46823084..46824632-chr16:46833245..46835025,2	MCF-7	breast:
19	chr16:46857437..46861981-chr16:46862572..46865905,5	MCF-7	breast:
20	chr16:46707389..46708210-chr16:46835449..46836029,2	MCF-7	breast:
21	chr16:46856407..46858707-chr16:46862664..46865192,2	K562	blood:
22	chr16:46841434..46846391-chr16:46846846..46850783,4	K562	blood:
23	chr16:46822185..46825488-chr16:46917726..46919426,3	K562	blood:
24	chr16:46822323..46826613-chr16:46862653..46866542,4	K562	blood:
25	chr16:46831873..46834182-chr16:46837803..46840106,2	K562	blood:

Variant related genes	Relation type
MYLK3	TF binding region
ENSG00000260782	TF binding region
MYLK3	CpG island
ENSG00000260782	CpG island
ENSG00000091651	chromatin interactions
ENSG00000140795	chromatin interactions
ENSG00000069329	chromatin interactions
ENSG00000166123	chromatin interactions
ENSG00000155330	chromatin interactions
ENSG00000260782	chromatin interactions
ENSG00000133627	chromatin interactions

Extended variants
information (count: 1036 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1036 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs808780	chr16:46820464-46820465	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188364131	chr16:46820551-46820552	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs541353656	chr16:46820611-46820612	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs200171491	chr16:46820647-46820648	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs376982468	chr16:46820662-46820663	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs533160745	chr16:46820745-46820746	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs545081733	chr16:46820790-46820791	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs192648606	chr16:46820843-46820844	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs537742203	chr16:46820853-46820854	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs559339077	chr16:46820854-46820855	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs563386502	chr16:46820886-46820887	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs185444437	chr16:46820917-46820918	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs189969801	chr16:46820951-46820952	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs71158900	chr16:46820980-46820981	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs529598804	chr16:46820981-46820982	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs78997269	chr16:46820992-46820993	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs398029246	chr16:46820994-46820995	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs571150202	chr16:46821003-46821004	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs140715987	chr16:46821047-46821048	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs535260944	chr16:46821090-46821091	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs538415192	chr16:46821171-46821172	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs369992006	chr16:46821187-46821188	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs373806316	chr16:46821228-46821229	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs567288406	chr16:46821242-46821243	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs542278890	chr16:46821245-46821246	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs112603747	chr16:46821246-46821247	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs143794401	chr16:46821280-46821281	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs539654834	chr16:46821362-46821363	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs191886054	chr16:46821393-46821394	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs569838552	chr16:46821399-46821400	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs184739066	chr16:46821406-46821407	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs553262894	chr16:46821452-46821453	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs376263278	chr16:46821491-46821492	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs574021746	chr16:46821493-46821494	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs372705127	chr16:46821523-46821524	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs574893327	chr16:46821563-46821564	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs112339247	chr16:46821616-46821617	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs189191974	chr16:46821617-46821618	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs151119316	chr16:46821647-46821648	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs541919832	chr16:46821680-46821681	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs370602179	chr16:46821682-46821683	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs375095755	chr16:46821684-46821685	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs369641602	chr16:46821729-46821730	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs533733978	chr16:46821751-46821752	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs8062662	chr16:46821776-46821777	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs563500655	chr16:46821781-46821782	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs547772368	chr16:46821820-46821821	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs200524558	chr16:46821822-46821823	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs575283280	chr16:46821885-46821886	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs576503802	chr16:46821900-46821901	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1015 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46791000-46823400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr16:46812800-46823400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:46819200-46822200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr16:46819200-46823400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr16:46819200-46823400	Weak transcription	HMEC	breast
6	chr16:46819400-46820800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr16:46819400-46821200	ZNF genes & repeats	GM12878-XiMat	blood
8	chr16:46819400-46822200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr16:46819400-46822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr16:46819400-46823000	Weak transcription	Stomach Mucosa	stomach
11	chr16:46819400-46823400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr16:46819400-46823400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr16:46819400-46823400	Weak transcription	NHEK	skin
14	chr16:46819600-46821800	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr16:46819600-46822200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr16:46819600-46822200	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr16:46819600-46822400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr16:46819600-46823400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr16:46819600-46823400	Weak transcription	Placenta	Placenta
20	chr16:46819800-46821600	Weak transcription	K562	blood
21	chr16:46819800-46822200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr16:46819800-46822200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr16:46819800-46822200	Weak transcription	HepG2	liver
24	chr16:46819800-46823400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr16:46820000-46821400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr16:46820200-46821400	Weak transcription	Fetal Heart	heart
27	chr16:46821000-46821600	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr16:46821000-46823400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr16:46821000-46823800	Enhancers	Primary B cells from peripheral blood	blood
30	chr16:46821200-46821600	Enhancers	GM12878-XiMat	blood
31	chr16:46821200-46823400	Weak transcription	Ovary	ovary
32	chr16:46821200-46824000	Enhancers	Primary B cells from cord blood	blood
33	chr16:46821400-46821600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr16:46821400-46821600	Enhancers	Fetal Heart	heart
35	chr16:46821400-46821800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr16:46821600-46821800	Enhancers	Primary T cells fromperipheralblood	blood
37	chr16:46821600-46821800	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr16:46821600-46821800	Enhancers	Spleen	Spleen
39	chr16:46821600-46821800	Enhancers	K562	blood
40	chr16:46821600-46821800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
41	chr16:46821600-46822000	Weak transcription	Fetal Heart	heart
42	chr16:46821600-46822400	Enhancers	Primary hematopoietic stem cells	blood
43	chr16:46821600-46823800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr16:46821600-46823800	Flanking Active TSS	GM12878-XiMat	blood
45	chr16:46821800-46822000	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr16:46821800-46822200	Weak transcription	K562	blood
47	chr16:46821800-46822400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr16:46821800-46823400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr16:46821800-46823400	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr16:46821800-46823400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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