Variant report

Variant	rs113589582
Chromosome Location	chr6:30431820-30431821
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:30431171-30431876	HL-60	blood:	n/a	n/a
2	ELF1	chr6:30431509-30432055	GM12878	blood:	n/a	n/a
3	GABPA	chr6:30431315-30431889	HL-60	blood:	n/a	n/a
4	SPI1	chr6:30431294-30431849	HL-60	blood:	n/a	n/a
5	POLR2A	chr6:30431183-30431865	HL-60	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:30431782-30431832	HCF	heart:	n/a
2	chr6:30431782-30431832	U87	brain:	n/a
3	chr6:30431770-30431820	HRCEpiC	kidney:	n/a
4	chr6:30431770-30431820	HEEpiC	esophagus:	n/a
5	chr6:30431782-30431832	ProgFib	skin:	n/a
6	chr6:30431782-30431832	SK-N-MC	brain:	n/a
7	chr6:30431782-30431832	PrEC	prostate:	n/a
8	chr6:30431782-30431832	LNCaP	prostate:	n/a
9	chr6:30431782-30431832	HRCEpiC	kidney:	n/a
10	chr6:30431782-30431832	NB4	blood:	n/a
11	chr6:30431770-30431820	NB4	blood:	n/a
12	chr6:30431782-30431832	HL-60	blood:	n/a
13	chr6:30431770-30431820	T-47D	breast:	n/a
14	chr6:30431770-30431820	SK-N-SH_RA	brain:	n/a
15	chr6:30431770-30431820	HMEC	breast:	n/a
16	chr6:30431770-30431820	GM12891	blood:	n/a
17	chr6:30431782-30431832	AG04450	lung:	fetal
18	chr6:30431782-30431832	SAEC	small airway:	n/a
19	chr6:30431782-30431832	H1-hESC	embryonic stem cell:	embryo
20	chr6:30431770-30431820	HNPCEpiC	eye:	n/a
21	chr6:30431770-30431820	MCF10A-Er-Src	breast:	n/a
22	chr6:30431770-30431820	HCF	heart:	n/a
23	chr6:30431770-30431820	HCPEpiC	choroid plexus:	n/a
24	chr6:30431782-30431832	Hepatocyte	liver:	n/a
25	chr6:30431782-30431832	AG10803	skin:	n/a
26	chr6:30431770-30431820	ovcar-3	ovarian:	n/a
27	chr6:30431782-30431832	A549	lung:	n/a
28	chr6:30431770-30431820	AG04450	lung:	fetal
29	chr6:30431782-30431832	SK-N-SH_RA	brain:	n/a
30	chr6:30431782-30431832	HMEC	breast:	n/a
31	chr6:30431782-30431832	NHDF-neo	bronchial:	n/a
32	chr6:30431770-30431820	A549	lung:	n/a
33	chr6:30431782-30431832	MCF10A-Er-Src	breast:	n/a
34	chr6:30431770-30431820	ProgFib	skin:	n/a
35	chr6:30431782-30431832	HepG2	liver:	n/a
36	chr6:30431770-30431820	HCT-116	colon:	n/a
37	chr6:30431782-30431832	PFSK-1	brain:	n/a
38	chr6:30431782-30431832	GM12892	blood:	n/a
39	chr6:30431770-30431820	PrEC	prostate:	n/a
40	chr6:30431782-30431832	HIPEpiC	eye:	n/a
41	chr6:30431782-30431832	SKMC	muscle:	n/a
42	chr6:30431770-30431820	NHBE	bronchial:	n/a
43	chr6:30431770-30431820	HRPEpiC	eye:	n/a
44	chr6:30431770-30431820	K562	blood:	n/a
45	chr6:30431782-30431832	BE2_C	brain:	n/a
46	chr6:30431770-30431820	RPTEC	kidney:	n/a
47	chr6:30431770-30431820	SKMC	muscle:	n/a
48	chr6:30431770-30431820	SK-N-SH	brain:	n/a
49	chr6:30431782-30431832	MCF-7	breast:	n/a
50	chr6:30431770-30431820	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr6:30418502..30422305-chr6:30429667..30432220,3	MCF-7	breast:
2	chr6:30431634..30434565-chr6:30582972..30585070,2	K562	blood:
3	chr6:30430770..30433095-chr6:30579406..30582231,2	K562	blood:
4	chr6:30431634..30435485-chr6:30582972..30586314,3	K562	blood:
5	chr6:30431267..30434167-chr6:30612886..30615610,2	MCF-7	breast:

No data

Variant related genes	Relation type
SUCLA2P1	TF binding region
TMPOP1	TF binding region
SUCLA2P1	CpG island
TMPOP1	CpG island
ENSG00000222894	Chromatin interaction
ENSG00000204564	Chromatin interaction
ENSG00000204569	Chromatin interaction
ENSG00000204568	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025667	chr6:30292845-30638066	Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	825 gene(s)	inside rSNPs	diseases
2	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
3	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
4	nsv601478	chr6:30383768-30438226	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	esv3336846	chr6:30420111-30432946	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
6	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
7	nsv884065	chr6:30430520-30446055	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
8	nsv884066	chr6:30430875-30440732	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
9	nsv884067	chr6:30430875-30446055	Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
10	nsv884068	chr6:30430875-30447987	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
11	nsv884069	chr6:30430875-30451474	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
12	nsv884070	chr6:30430875-30472772	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30429800-30434200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
2	chr6:30430800-30432400	Bivalent Enhancer	Fetal Thymus	thymus
3	chr6:30431000-30432000	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
4	chr6:30431000-30432000	Bivalent Enhancer	Dnd41	blood
5	chr6:30431000-30432000	Bivalent Enhancer	GM12878-XiMat	blood
6	chr6:30431000-30432000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
7	chr6:30431000-30432200	Enhancers	Gastric	stomach
8	chr6:30431000-30432400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
9	chr6:30431000-30432400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
10	chr6:30431000-30432400	Bivalent Enhancer	Colon Smooth Muscle	Colon
11	chr6:30431000-30432400	Enhancers	Pancreas	Pancrea
12	chr6:30431000-30432400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
13	chr6:30431000-30432600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
14	chr6:30431000-30432600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:30431000-30432600	Bivalent Enhancer	Adipose Nuclei	Adipose
16	chr6:30431200-30432000	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
17	chr6:30431200-30432000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr6:30431200-30432000	Bivalent Enhancer	Brain Anterior Caudate	brain
19	chr6:30431200-30432200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
20	chr6:30431200-30432200	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
21	chr6:30431200-30432200	Flanking Bivalent TSS/Enh	Primary T helper naive cells from peripheral blood	blood
22	chr6:30431200-30432400	Bivalent Enhancer	Fetal Heart	heart
23	chr6:30431200-30432600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr6:30431400-30432000	Flanking Active TSS	Primary B cells from cord blood	blood
25	chr6:30431400-30432000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
26	chr6:30431400-30432000	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
27	chr6:30431400-30432000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
28	chr6:30431400-30432000	Bivalent Enhancer	Liver	Liver
29	chr6:30431400-30432000	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
30	chr6:30431400-30432000	Bivalent Enhancer	Duodenum Mucosa	Duodenum
31	chr6:30431400-30432200	Bivalent Enhancer	Fetal Stomach	stomach
32	chr6:30431400-30432400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:30431400-30432400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr6:30431400-30432400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
35	chr6:30431400-30432400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr6:30431400-30432400	Bivalent Enhancer	Fetal Muscle Leg	muscle
37	chr6:30431400-30432400	Bivalent Enhancer	Placenta	Placenta
38	chr6:30431400-30432600	Bivalent Enhancer	Fetal Intestine Small	intestine
39	chr6:30431400-30432800	Bivalent Enhancer	Spleen	Spleen
40	chr6:30431400-30433000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr6:30431400-30434000	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
42	chr6:30431600-30432000	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr6:30431600-30432000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr6:30431600-30432000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr6:30431600-30432000	Bivalent Enhancer	Brain Hippocampus Middle	brain
46	chr6:30431600-30432000	Bivalent Enhancer	Psoas Muscle	Psoas
47	chr6:30431600-30432000	Flanking Bivalent TSS/Enh	Right Ventricle	heart
48	chr6:30431600-30432000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
49	chr6:30431600-30432000	Flanking Bivalent TSS/Enh	HSMM	muscle
50	chr6:30431600-30432200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain

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