Variant report

Variant	rs183984949
Chromosome Location	chr6:34385660-34385661
allele	A/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:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:34206861..34220421-chr6:34379359..34386848,24	K562	blood:
2	chr6:34111438..34113496-chr6:34384142..34385841,2	MCF-7	breast:
3	chr6:34379707..34381540-chr6:34384149..34385889,2	MCF-7	breast:
4	chr6:34204321..34205956-chr6:34384818..34387597,2	K562	blood:
5	chr6:34385629..34388479-chr6:34571535..34574090,2	K562	blood:
6	chr6:34356693..34361584-chr6:34376924..34385699,12	K562	blood:
7	chr6:34212124..34218246-chr6:34379945..34387655,19	K562	blood:
8	chr6:34379437..34382145-chr6:34384252..34386142,2	MCF-7	breast:
9	chr6:34384595..34386120-chr6:35175075..35178043,2	K562	blood:
10	chr6:34162021..34165758-chr6:34380623..34387316,6	K562	blood:
11	chr6:34358377..34360251-chr6:34384641..34386602,2	MCF-7	breast:
12	chr6:34306948..34308563-chr6:34383951..34386778,2	K562	blood:
13	chr6:34211137..34213160-chr6:34384345..34386352,2	MCF-7	breast:
14	chr6:34218726..34220421-chr6:34383770..34386594,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000186577	Chromatin interaction
ENSG00000137309	Chromatin interaction
ENSG00000272325	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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	nsv1022844	chr6:34317219-35060519	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv538195	chr6:34317219-35060519	Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	esv2758046	chr6:34382492-34714677	Genic enhancers Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	esv2759418	chr6:34382492-34714677	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv981133	chr6:34385156-34393521	Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34372400-34389400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:34379200-34391800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr6:34381800-34391000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr6:34382000-34388000	Strong transcription	Dnd41	blood
5	chr6:34382000-34390000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:34382000-34391600	Strong transcription	NHEK	skin
7	chr6:34382000-34392000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:34382000-34392000	Strong transcription	Primary T cells from cord blood	blood
9	chr6:34382400-34389400	Strong transcription	K562	blood
10	chr6:34382400-34389600	Weak transcription	Fetal Brain Male	brain
11	chr6:34382400-34391800	Strong transcription	NHDF-Ad	bronchial
12	chr6:34382400-34392000	Strong transcription	H1 Cell Line	embryonic stem cell
13	chr6:34382400-34392000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:34382400-34392000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr6:34382600-34387600	Weak transcription	Fetal Kidney	kidney
16	chr6:34382600-34387800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:34382600-34392000	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr6:34382800-34386000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr6:34383000-34391000	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr6:34383000-34392200	Weak transcription	Right Atrium	heart
21	chr6:34383200-34389200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr6:34383200-34389400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr6:34383200-34391600	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr6:34383200-34391600	Strong transcription	Fetal Thymus	thymus
25	chr6:34383400-34389400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:34383400-34390000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr6:34383400-34390000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:34383400-34390000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr6:34383400-34392000	Strong transcription	H9 Cell Line	embryonic stem cell
30	chr6:34383400-34392000	Strong transcription	Fetal Lung	lung
31	chr6:34383400-34392600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr6:34383400-34392600	Strong transcription	Lung	lung
33	chr6:34383600-34386800	Strong transcription	Brain Germinal Matrix	brain
34	chr6:34383600-34389000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr6:34383600-34389400	Strong transcription	GM12878-XiMat	blood
36	chr6:34383600-34390200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr6:34383600-34391200	Strong transcription	Osteobl	bone
38	chr6:34383600-34391400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr6:34383600-34391400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:34383600-34391400	Strong transcription	Fetal Muscle Trunk	muscle
41	chr6:34383600-34391600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr6:34383600-34391600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr6:34383600-34392000	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr6:34383600-34392000	Strong transcription	Fetal Brain Female	brain
45	chr6:34383600-34392000	Strong transcription	Fetal Intestine Small	intestine
46	chr6:34383600-34392000	Strong transcription	Thymus	Thymus
47	chr6:34383600-34392200	Strong transcription	Fetal Muscle Leg	muscle
48	chr6:34383600-34392600	Strong transcription	Fetal Intestine Large	intestine
49	chr6:34383800-34386000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr6:34383800-34386800	Strong transcription	Primary hematopoietic stem cells	blood

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