Variant report

Variant	rs3786837
Chromosome Location	chr19:39172042-39172043
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No data

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

No.	Distal block	Cell Line	Cell type
1	chr19:39169983..39173495-chr19:39173704..39177059,4	K562	blood:
2	chr19:39157020..39159393-chr19:39170595..39173839,3	MCF-7	breast:
3	chr19:39165775..39169288-chr19:39170285..39176842,12	K562	blood:
4	chr19:39171849..39173429-chr19:39204483..39206765,2	MCF-7	breast:
5	chr19:39170783..39173793-chr19:39174469..39178078,4	MCF-7	breast:
6	chr19:39170809..39173774-chr19:39199187..39201318,2	K562	blood:
7	chr19:39127720..39130630-chr19:39171842..39174626,3	MCF-7	breast:
8	chr19:39141235..39143219-chr19:39170803..39172948,2	K562	blood:

No data

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10403540	0.84[EUR][1000 genomes]
rs10406778	0.92[EUR][1000 genomes]
rs10415219	0.92[CEU][hapmap]
rs10415646	0.87[EUR][1000 genomes]
rs10421560	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs11083475	0.93[CEU][hapmap];0.88[EUR][1000 genomes]
rs12460849	0.93[CEU][hapmap]
rs12462270	0.96[CEU][hapmap];0.84[EUR][1000 genomes]
rs13343794	0.87[EUR][1000 genomes]
rs13344413	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.86[EUR][1000 genomes]
rs16972767	0.96[CEU][hapmap]
rs2279144	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs2303040	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs28488032	0.85[EUR][1000 genomes]
rs28624276	0.86[EUR][1000 genomes]
rs3745859	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs3786835	0.93[CEU][hapmap]
rs3786839	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3786845	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs3786848	0.84[EUR][1000 genomes]
rs3786851	0.92[CEU][hapmap];0.83[EUR][1000 genomes]
rs56113315	0.85[EUR][1000 genomes]
rs62121816	0.88[EUR][1000 genomes]
rs62121818	0.92[EUR][1000 genomes]
rs7251903	0.93[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7252589	0.87[EUR][1000 genomes]
rs7254100	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs8107416	0.88[CEU][hapmap]
rs883394	0.85[EUR][1000 genomes]
rs883433	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs979971	0.92[CEU][hapmap]
rs979972	0.93[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833826	chr19:38945106-39184547	Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
2	nsv833827	chr19:38993054-39184547	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	nsv833828	chr19:39084759-39257979	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv1057899	chr19:39088319-39475493	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
5	nsv1057901	chr19:39112486-39174332	Genic enhancers Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39160400-39173400	Weak transcription	Brain Germinal Matrix	brain
2	chr19:39161200-39176000	Weak transcription	Fetal Brain Male	brain
3	chr19:39161200-39176000	Weak transcription	Fetal Brain Female	brain
4	chr19:39162200-39173400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr19:39162800-39173200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr19:39164400-39172600	Enhancers	Small Intestine	intestine
7	chr19:39164400-39200200	Genic enhancers	Fetal Intestine Small	intestine
8	chr19:39164600-39173800	Genic enhancers	HepG2	liver
9	chr19:39164600-39178200	Enhancers	Primary T cells fromperipheralblood	blood
10	chr19:39164800-39172600	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr19:39164800-39173800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr19:39164800-39177600	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr19:39164800-39179200	Enhancers	Pancreas	Pancrea
14	chr19:39164800-39179800	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr19:39164800-39183800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr19:39165000-39174200	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr19:39165400-39172600	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr19:39165400-39178200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr19:39165600-39174000	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr19:39166000-39178200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr19:39166200-39172400	Genic enhancers	NHEK	skin
22	chr19:39166200-39173800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr19:39166200-39173800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr19:39166400-39173800	Genic enhancers	HMEC	breast
25	chr19:39166600-39173400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr19:39167200-39173600	Enhancers	Stomach Mucosa	stomach
27	chr19:39167200-39173800	Genic enhancers	Fetal Intestine Large	intestine
28	chr19:39167200-39175600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr19:39167400-39173600	Genic enhancers	Lung	lung
30	chr19:39167400-39173800	Genic enhancers	NHLF	lung
31	chr19:39167400-39174400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr19:39167400-39180800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr19:39167600-39173400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr19:39167600-39173800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr19:39167600-39174000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr19:39167800-39173000	Weak transcription	Fetal Lung	lung
37	chr19:39167800-39173200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr19:39167800-39174000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr19:39167800-39174000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr19:39167800-39175200	Weak transcription	Primary T cells from cord blood	blood
41	chr19:39168000-39173200	Weak transcription	Aorta	Aorta
42	chr19:39168400-39177400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr19:39168800-39173800	Enhancers	Right Ventricle	heart
44	chr19:39169000-39172200	Genic enhancers	NH-A	brain
45	chr19:39169000-39174000	Genic enhancers	HSMM	muscle
46	chr19:39169200-39174000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr19:39169200-39174200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr19:39169200-39181000	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr19:39169400-39172400	Transcr. at gene 5' and 3'	A549	lung
50	chr19:39169400-39173600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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