Variant report

Variant	rs57495074
Chromosome Location	chr4:16226944-16226945
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:40)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:40 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr4:16226840-16226990	HPAF	blood vessel:	n/a	n/a
2	CTCF	chr4:16226900-16227050	AG10803	skin:	n/a	n/a
3	CEBPB	chr4:16226766-16227087	K562	blood:	n/a	n/a
4	CTCF	chr4:16226940-16227090	HPAF	blood vessel:	n/a	n/a
5	EP300	chr4:16226813-16227177	GM12878	blood:	n/a	chr4:16226924-16226932
6	CTCF	chr4:16226935-16227101	IMR90	lung:	n/a	n/a
7	POLR2A	chr4:16226799-16229901	GM12891	blood:	n/a	n/a
8	CTCF	chr4:16226880-16227030	HCM	heart:	n/a	n/a
9	E2F4	chr4:16226509-16227090	MCF10A-Er-Src	breast:	n/a	n/a
10	CTCF	chr4:16226904-16227500	K562	blood:	n/a	chr4:16227285-16227293
11	POLR2A	chr4:16226421-16229959	MCF10A-Er-Src	breast:	n/a	n/a
12	HCFC1	chr4:16226663-16228826	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr4:16226920-16227070	NHDF-neo	bronchial:	n/a	n/a
14	ARID3A	chr4:16226793-16227076	K562	blood:	n/a	n/a
15	CTCF	chr4:16226860-16227010	AG04450	lung:	n/a	n/a
16	CEBPB	chr4:16226759-16227141	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr4:16226940-16227090	AG04450	lung:	n/a	n/a
18	CTCF	chr4:16226840-16226990	HMF	breast:	n/a	n/a
19	CTCF	chr4:16226920-16227070	AG09319	gingival:	n/a	n/a
20	TBP	chr4:16226575-16227520	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr4:16226940-16227090	HCFaa	heart:	n/a	n/a
22	TBP	chr4:16226606-16227206	GM12878	blood:	n/a	n/a
23	ATF2	chr4:16226676-16227202	GM12878	blood:	n/a	n/a
24	POLR2A	chr4:16226639-16229966	PBDE	blood:	n/a	n/a
25	CUX1	chr4:16226802-16227046	K562	blood:	n/a	n/a
26	CEBPB	chr4:16226750-16227074	IMR90	lung:	n/a	n/a
27	RAD21	chr4:16226936-16227055	IMR90	lung:	n/a	n/a
28	CTCF	chr4:16226880-16227030	HMF	breast:	n/a	n/a
29	CTCF	chr4:16226900-16227050	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr4:16226880-16227030	AoAF	blood vessel:	n/a	n/a
31	CHD1	chr4:16226879-16227693	GM12878	blood:	n/a	n/a
32	CTCF	chr4:16226880-16227030	AG10803	skin:	n/a	n/a
33	JUND	chr4:16226794-16227073	K562	blood:	n/a	n/a
34	CTCF	chr4:16226920-16227070	BJ	skin:	n/a	n/a
35	TBL1XR1	chr4:16226346-16227606	K562	blood:	n/a	n/a
36	POLR2A	chr4:16226783-16230420	Raji	blood:	n/a	n/a
37	CTCF	chr4:16226880-16227030	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr4:16226880-16227030	HPF	lung:	n/a	n/a
39	CTCF	chr4:16226900-16227050	HRE	kidney:	n/a	n/a
40	JUND	chr4:16226778-16227085	HepG2	liver:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr4:16212529..16219737-chr4:16225844..16229602,8	MCF-7	breast:
2	chr4:15002785..15006911-chr4:16226901..16230678,5	K562	blood:
3	chr4:15681714..15684664-chr4:16226494..16229781,3	K562	blood:

No data

Variant related genes	Relation type
TAPT1-AS1	TF binding region
ENSG00000118564	Chromatin interaction
ENSG00000169762	Chromatin interaction
ENSG00000247624	Chromatin interaction
ENSG00000137449	Chromatin interaction
ENSG00000237765	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004821	chr4:16055996-16830629	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv537046	chr4:16055996-16830629	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv537047	chr4:16182060-16375787	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv878720	chr4:16222046-16242215	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv537048	chr4:16226406-16375787	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	esv3405372	chr4:16226679-16229727	Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	esv3489117	chr4:16226904-16229802	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	esv3489118	chr4:16226904-16229802	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 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	chr4:16208800-16227200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:16224400-16227000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr4:16224400-16227000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:16224400-16227200	Enhancers	Small Intestine	intestine
5	chr4:16224600-16227000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr4:16224600-16227000	Flanking Active TSS	Liver	Liver
7	chr4:16224800-16227600	Flanking Active TSS	Primary hematopoietic stem cells	blood
8	chr4:16225000-16227200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
9	chr4:16225200-16227200	Flanking Active TSS	Primary T cells from cord blood	blood
10	chr4:16225600-16227000	Flanking Active TSS	Brain Substantia Nigra	brain
11	chr4:16225600-16227000	Flanking Active TSS	Hela-S3	cervix
12	chr4:16225600-16227200	Flanking Active TSS	Brain Angular Gyrus	brain
13	chr4:16225600-16227400	Flanking Active TSS	Primary B cells from cord blood	blood
14	chr4:16225600-16227600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
15	chr4:16225600-16230800	Active TSS	A549	lung
16	chr4:16225800-16227000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr4:16225800-16227000	Flanking Active TSS	Fetal Brain Female	brain
18	chr4:16225800-16227000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
19	chr4:16225800-16227000	Flanking Active TSS	Rectal Smooth Muscle	rectum
20	chr4:16225800-16227200	Flanking Active TSS	Adipose Nuclei	Adipose
21	chr4:16225800-16227400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
22	chr4:16225800-16227400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
23	chr4:16225800-16227400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
24	chr4:16225800-16227400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr4:16225800-16227600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
26	chr4:16225800-16230000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr4:16226000-16227000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:16226000-16227000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr4:16226000-16227000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr4:16226000-16227000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
31	chr4:16226000-16227000	Flanking Active TSS	Fetal Kidney	kidney
32	chr4:16226000-16227400	Flanking Active TSS	Brain Germinal Matrix	brain
33	chr4:16226000-16227600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr4:16226200-16227000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr4:16226200-16227000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr4:16226200-16227200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr4:16226200-16227200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:16226200-16227200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr4:16226200-16227200	Flanking Active TSS	Fetal Heart	heart
40	chr4:16226200-16227200	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr4:16226200-16227400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:16226200-16227600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:16226200-16227600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
44	chr4:16226200-16229600	Active TSS	Right Atrium	heart
45	chr4:16226400-16227000	Flanking Active TSS	Primary B cells from peripheral blood	blood
46	chr4:16226400-16227000	Weak transcription	Placenta	Placenta
47	chr4:16226400-16227000	Weak transcription	Stomach Mucosa	stomach
48	chr4:16226400-16227000	Flanking Active TSS	Dnd41	blood
49	chr4:16226400-16227200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr4:16226400-16227200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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