Variant report

Variant	rs67844017
Chromosome Location	chr6:37479853-37479854
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:37474227..37476021-chr6:37478764..37481266,2	K562	blood:
2	chr6:37479736..37486031-chr6:37501228..37507298,5	K562	blood:
3	chr6:37462097..37469080-chr6:37478016..37487473,13	K562	blood:
4	chr6:37479736..37482449-chr6:37501228..37503661,2	K562	blood:

Variant related genes	Relation type
ENSG00000204110	Chromatin interaction
ENSG00000198937	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs13193757	0.83[ASN][1000 genomes]
rs1776459	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55939502	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56145403	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs58700472	0.86[EUR][1000 genomes]
rs60421847	0.81[EUR][1000 genomes]
rs67409335	0.87[ASN][1000 genomes]
rs72855417	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs883373	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752124	chr6:37416219-37680622	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1016310	chr6:37473075-37528469	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37468000-37483600	Enhancers	Fetal Thymus	thymus
2	chr6:37471200-37483600	Weak transcription	Spleen	Spleen
3	chr6:37473800-37482200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:37476200-37483600	Enhancers	Thymus	Thymus
5	chr6:37476400-37481200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr6:37476600-37480400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:37476800-37482200	Weak transcription	GM12878-XiMat	blood
8	chr6:37477000-37480400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr6:37477400-37480200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr6:37477400-37480200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr6:37477800-37480000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr6:37478600-37480400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
13	chr6:37478600-37481000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:37478800-37481600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr6:37478800-37481800	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr6:37478800-37482200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr6:37478800-37482400	Enhancers	Primary T cells from cord blood	blood
18	chr6:37478800-37482400	Enhancers	Primary T cells fromperipheralblood	blood
19	chr6:37478800-37482400	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr6:37479000-37482200	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr6:37479000-37486400	Enhancers	Fetal Brain Female	brain
22	chr6:37479000-37486800	Enhancers	Fetal Brain Male	brain
23	chr6:37479200-37480400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr6:37479200-37483800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr6:37479400-37480000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:37479400-37480200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:37479400-37480200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr6:37479400-37482200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:37479400-37483200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr6:37479400-37483600	Weak transcription	Right Atrium	heart
31	chr6:37479400-37486200	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr6:37479600-37481400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:37479600-37481400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
34	chr6:37479600-37481800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
35	chr6:37479600-37482400	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr6:37479800-37480000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
37	chr6:37479800-37480200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr6:37479800-37481000	Bivalent Enhancer	Fetal Muscle Leg	muscle
39	chr6:37479800-37481200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
40	chr6:37479800-37481200	Weak transcription	Brain Germinal Matrix	brain
41	chr6:37479800-37481200	Bivalent Enhancer	Placenta	Placenta
42	chr6:37479800-37481400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
43	chr6:37479800-37481600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
44	chr6:37479800-37481600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
45	chr6:37479800-37481600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
46	chr6:37479800-37481800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell

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