Variant report

Variant	rs6927499
Chromosome Location	chr6:144161744-144161745
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXA1	chr6:144161596-144161961	HepG2	liver:	n/a	n/a
2	RCOR1	chr6:144161730-144162112	K562	blood:	n/a	n/a
3	FOXA1	chr6:144161687-144161805	T-47D	breast:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:144152743..144156457-chr6:144158826..144162488,4	K562	blood:
2	chr6:144157133..144162462-chr6:144162661..144166157,6	MCF-7	breast:
3	chr6:144138025..144143695-chr6:144157697..144164178,7	K562	blood:
4	chr6:144159147..144162101-chr6:144162697..144165631,5	K562	blood:
5	chr6:144093414..144096259-chr6:144161351..144164009,2	K562	blood:

No data

Variant related genes	Relation type
LTV1	TF binding region
ENSG00000135521	Chromatin interaction
ENSG00000112419	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs2277078	0.85[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	esv3408554	chr6:144106707-144369589	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1034894	chr6:144148566-144170036	Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	10 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	chr6:144122200-144163600	Weak transcription	Colonic Mucosa	Colon
2	chr6:144122200-144163600	Weak transcription	Fetal Kidney	kidney
3	chr6:144125600-144163600	Weak transcription	Psoas Muscle	Psoas
4	chr6:144125800-144163600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr6:144128800-144163600	Weak transcription	HSMMtube	muscle
6	chr6:144129200-144163600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:144129200-144163600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr6:144129600-144163600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr6:144130200-144163400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr6:144130200-144163800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr6:144134000-144163800	Weak transcription	Aorta	Aorta
12	chr6:144134000-144163800	Weak transcription	Esophagus	oesophagus
13	chr6:144134000-144164000	Weak transcription	Gastric	stomach
14	chr6:144136600-144163600	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr6:144140800-144163400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:144142200-144164000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr6:144143000-144163400	Weak transcription	Fetal Stomach	stomach
18	chr6:144144200-144164000	Weak transcription	Lung	lung
19	chr6:144145200-144163600	Weak transcription	NH-A	brain
20	chr6:144145200-144163600	Weak transcription	NHEK	skin
21	chr6:144146200-144163600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:144146400-144163600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr6:144146400-144163600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr6:144147800-144163400	Weak transcription	HUVEC	blood vessel
25	chr6:144150000-144163400	Weak transcription	Fetal Muscle Trunk	muscle
26	chr6:144150000-144164000	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr6:144150600-144163000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr6:144150800-144163600	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr6:144150800-144163600	Weak transcription	Adipose Nuclei	Adipose
30	chr6:144150800-144163600	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr6:144151800-144163600	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr6:144153200-144163800	Weak transcription	Placenta	Placenta
33	chr6:144157000-144163800	Weak transcription	Pancreas	Pancrea
34	chr6:144158800-144162200	Enhancers	Stomach Mucosa	stomach
35	chr6:144160000-144163600	Weak transcription	Liver	Liver
36	chr6:144160400-144163600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr6:144160400-144163600	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr6:144160600-144163600	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr6:144160800-144163400	Weak transcription	Fetal Muscle Leg	muscle
40	chr6:144160800-144163600	Weak transcription	Duodenum Mucosa	Duodenum
41	chr6:144160800-144163600	Weak transcription	HepG2	liver
42	chr6:144160800-144163600	Weak transcription	Osteobl	bone
43	chr6:144160800-144164000	Weak transcription	Small Intestine	intestine
44	chr6:144161000-144162200	Weak transcription	Fetal Intestine Small	intestine
45	chr6:144161000-144163600	Weak transcription	Fetal Intestine Large	intestine
46	chr6:144161400-144163600	Weak transcription	Duodenum Smooth Muscle	Duodenum

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