Variant report

Variant	rs774777
Chromosome Location	chr3:111763052-111763053
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:111762244..111763263-chr3:111830391..111831101,4	MCF-7	breast:
2	chr3:111752540..111756075-chr3:111760637..111763869,3	MCF-7	breast:
3	chr3:111707963..111708464-chr3:111762324..111763155,2	K562	blood:
4	chr3:111707324..111708507-chr3:111762237..111763099,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000176040	Chromatin interaction

rs_ID	r²[population]
rs1627007	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs1688285	1.00[AFR][1000 genomes]
rs1725753	1.00[AFR][1000 genomes]
rs340162	1.00[YRI][hapmap]
rs4383485	1.00[YRI][hapmap]
rs4611790	1.00[YRI][hapmap]
rs4682363	1.00[YRI][hapmap]
rs6796382	1.00[YRI][hapmap]
rs7642708	1.00[YRI][hapmap]
rs7653647	1.00[YRI][hapmap]
rs9755969	1.00[YRI][hapmap]

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111756200-111763200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr3:111757600-111767800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:111760600-111766600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr3:111760600-111767600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr3:111760600-111767600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:111761400-111763200	Enhancers	Stomach Mucosa	stomach
7	chr3:111762200-111763200	Weak transcription	Fetal Intestine Small	intestine
8	chr3:111762200-111764000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr3:111762400-111763400	Enhancers	Fetal Thymus	thymus
10	chr3:111762400-111763800	Enhancers	HUVEC	blood vessel
11	chr3:111762400-111771000	Weak transcription	Gastric	stomach
12	chr3:111762600-111763400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr3:111762600-111765600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr3:111762600-111767800	Weak transcription	Fetal Intestine Large	intestine
15	chr3:111762800-111763200	Active TSS	Aorta	Aorta
16	chr3:111762800-111763200	Enhancers	Thymus	Thymus
17	chr3:111762800-111763200	Bivalent/Poised TSS	GM12878-XiMat	blood
18	chr3:111763000-111763200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:111763000-111763200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr3:111763000-111763200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr3:111763000-111763200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr3:111763000-111763200	Enhancers	Hela-S3	cervix
23	chr3:111763000-111763200	Enhancers	Osteobl	bone
24	chr3:111763000-111763400	Enhancers	A549	lung
25	chr3:111763000-111763400	Enhancers	Dnd41	blood
26	chr3:111763000-111765600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:111763000-111765600	Weak transcription	HMEC	breast
28	chr3:111763000-111765600	Weak transcription	NHEK	skin
29	chr3:111763000-111765800	Weak transcription	NH-A	brain
30	chr3:111763000-111766400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr3:111763000-111767400	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr3:111763000-111767600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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