Variant report

Variant	rs142997360
Chromosome Location	chr4:129785984-129785985
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:129729198..129732287-chr4:129784290..129787717,5	K562	blood:
2	chr4:129784722..129788908-chr4:129789150..129792648,4	K562	blood:
3	chr4:129729755..129733795-chr4:129783264..129786218,5	MCF-7	breast:
4	chr4:129729294..129734540-chr4:129782960..129791658,9	K562	blood:

Variant related genes	Relation type
ENSG00000077684	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869258	chr4:129191619-130138148	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
2	nsv517249	chr4:129738328-129927804	Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv1026938	chr4:129770961-129936205	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv1030513	chr4:129770961-129965026	Strong transcription Genic enhancers Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv870175	chr4:129771718-129937945	Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv1026772	chr4:129773881-129936205	ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
7	nsv461637	chr4:129774375-129924977	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
8	nsv595397	chr4:129774375-129924977	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
9	nsv461638	chr4:129774375-129927804	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
10	nsv595398	chr4:129774375-129927804	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
11	nsv1018994	chr4:129775612-129933968	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
12	nsv4504	chr4:129777368-129803959	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
13	nsv1034996	chr4:129777825-129905255	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
14	nsv537249	chr4:129777825-129905255	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
15	nsv1022446	chr4:129778025-129905116	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
16	nsv537250	chr4:129778025-129905116	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
17	nsv1030296	chr4:129778025-129920680	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
18	nsv537251	chr4:129778025-129920680	Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
19	esv2830419	chr4:129785483-129905256	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
20	nsv533785	chr4:129785683-129857992	ZNF genes & repeats Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:129753600-129798600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:129753800-129795000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:129763000-129787200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:129763600-129786600	Strong transcription	Fetal Intestine Large	intestine
5	chr4:129772600-129786000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
6	chr4:129773200-129794000	Strong transcription	K562	blood
7	chr4:129774000-129788600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr4:129776400-129796200	Strong transcription	Dnd41	blood
9	chr4:129779600-129809800	Weak transcription	Small Intestine	intestine
10	chr4:129779800-129793200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr4:129782400-129786800	Strong transcription	Fetal Intestine Small	intestine
12	chr4:129782400-129787200	Weak transcription	Hela-S3	cervix
13	chr4:129782800-129786800	Strong transcription	Fetal Stomach	stomach
14	chr4:129783400-129789200	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr4:129783400-129800600	Weak transcription	Fetal Kidney	kidney
16	chr4:129783600-129789600	Weak transcription	HMEC	breast
17	chr4:129784000-129788200	Weak transcription	Placenta	Placenta
18	chr4:129784000-129788600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:129784000-129789800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:129784200-129786000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr4:129784200-129786000	Weak transcription	HepG2	liver
22	chr4:129784200-129788400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:129784200-129788400	Weak transcription	Ovary	ovary
24	chr4:129784200-129790000	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr4:129784200-129790800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:129784400-129786000	Weak transcription	Aorta	Aorta
27	chr4:129784400-129786200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
28	chr4:129784400-129786400	Strong transcription	Pancreas	Pancrea
29	chr4:129784400-129787400	Weak transcription	Right Atrium	heart
30	chr4:129784400-129788400	Weak transcription	Brain Germinal Matrix	brain
31	chr4:129784400-129792000	Weak transcription	Colonic Mucosa	Colon
32	chr4:129784400-129792600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr4:129784400-129799200	Weak transcription	Fetal Brain Male	brain
34	chr4:129784600-129786000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:129784600-129786000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr4:129784600-129786000	Weak transcription	Gastric	stomach
37	chr4:129784600-129786000	Weak transcription	Left Ventricle	heart
38	chr4:129784600-129786200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:129784600-129786400	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr4:129784600-129787200	Strong transcription	A549	lung
41	chr4:129784600-129787600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr4:129784600-129788200	Weak transcription	Lung	lung
43	chr4:129784600-129789800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr4:129784600-129791000	Weak transcription	Esophagus	oesophagus
45	chr4:129784600-129791400	Weak transcription	Spleen	Spleen
46	chr4:129784600-129792600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr4:129784600-129794000	Strong transcription	Duodenum Smooth Muscle	Duodenum
48	chr4:129784600-129795000	Strong transcription	Primary B cells from cord blood	blood
49	chr4:129784600-129798400	Strong transcription	Fetal Thymus	thymus
50	chr4:129784800-129786000	Strong transcription	HUES6 Cell Line	embryonic stem cell

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