Variant report

Variant	rs187533707
Chromosome Location	chr7:100025308-100025309
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7)
CpG islands
(count:0)
Chromatin interactive
region (count:51)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:7 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	E2F6	chr7:100025267-100027710	H1-hESC	embryonic stem cell:	n/a	chr7:100025863-100025870 chr7:100026011-100026025 chr7:100025863-100025870 chr7:100027410-100027419 chr7:100025861-100025872 chr7:100025862-100025871 chr7:100025941-100025950 chr7:100027323-100027332 chr7:100026924-100026933 chr7:100025862-100025870 chr7:100025862-100025874 chr7:100025863-100025870
2	HCFC1	chr7:100025291-100027869	Hela-S3	cervix:	n/a	n/a
3	CBX3	chr7:100025288-100027711	K562	blood:	n/a	n/a
4	MXI1	chr7:100025300-100029158	SK-N-SH	brain:	n/a	n/a
5	POLR2A	chr7:100025291-100025328	HepG2	liver:	n/a	n/a
6	MAX	chr7:100025276-100028297	HCT-116	colon:	n/a	chr7:100027575-100027585 chr7:100026944-100026953
7	STAT5A	chr7:100025303-100028840	GM12878	blood:	n/a	chr7:100027549-100027561 chr7:100026130-100026138

No data

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:100024810..100029555-chr7:100269638..100276218,15	K562	blood:
2	chr7:100025040..100027512-chr7:100201980..100203554,3	K562	blood:
3	chr7:100024854..100029212-chr7:100238393..100241596,5	K562	blood:
4	chr7:100025071..100027924-chr7:100727777..100730095,3	K562	blood:
5	chr7:100024700..100032514-chr7:100067180..100083143,31	K562	blood:
6	chr7:100024644..100031194-chr7:100062394..100068680,9	K562	blood:
7	chr7:99677060..99680949-chr7:100024846..100027547,5	MCF-7	breast:
8	chr7:99677846..99681399-chr7:100025174..100029012,4	K562	blood:
9	chr7:100025231..100027840-chr7:100303669..100306614,3	K562	blood:
10	chr4:164413226..164415880-chr7:100024994..100026878,2	MCF-7	breast:
11	chr7:99753605..99756389-chr7:100024404..100026585,2	MCF-7	breast:
12	chr7:99695452..99699124-chr7:100025277..100027831,3	MCF-7	breast:
13	chr7:99697437..99703178-chr7:100024624..100029482,10	K562	blood:
14	chr7:100025223..100026949-chr7:104653159..104655060,2	MCF-7	breast:
15	chr7:100009272..100011233-chr7:100024353..100026026,2	MCF-7	breast:
16	chr1:11967024..11970880-chr7:100024808..100027879,3	K562	blood:
17	chr7:100024823..100028490-chr7:100199635..100204792,9	MCF-7	breast:
18	chr7:100004091..100007847-chr7:100024893..100029911,8	MCF-7	breast:
19	chr7:100024866..100028113-chr7:100485356..100489963,5	MCF-7	breast:
20	chr7:99696789..99700792-chr7:100024893..100031468,10	K562	blood:
21	chr7:100024969..100026513-chr7:100273974..100276218,2	MCF-7	breast:
22	chr7:100009832..100015861-chr7:100024427..100028524,9	MCF-7	breast:
23	chr7:99965641..99971124-chr7:100025245..100028820,5	MCF-7	breast:
24	chr7:100025163..100029050-chr7:100284721..100290800,5	MCF-7	breast:
25	chr7:100024988..100028445-chr7:100180808..100186978,10	K562	blood:
26	chr7:100024682..100026645-chr7:100273094..100274953,2	K562	blood:
27	chr7:100025040..100027312-chr7:100198003..100200781,2	K562	blood:
28	chr7:99998688..100005691-chr7:100025198..100032529,13	K562	blood:
29	chr7:100024981..100028086-chr7:100074705..100078040,4	MCF-7	breast:
30	chr7:100023646..100028399-chr7:100166149..100169452,5	K562	blood:
31	chr7:100025040..100028858-chr7:100198464..100203953,10	K562	blood:
32	chr7:100025028..100029218-chr7:100206824..100213289,7	K562	blood:
33	chr7:99723158..99726590-chr7:100025016..100029006,5	K562	blood:
34	chr7:99717030..99721378-chr7:100025256..100028946,7	MCF-7	breast:
35	chr7:99723171..99726242-chr7:100025216..100028355,4	MCF-7	breast:
36	chr7:99754046..99756900-chr7:100023826..100027525,3	MCF-7	breast:
37	chr7:99515753..99518653-chr7:100025054..100026663,2	K562	blood:
38	chr7:100025223..100027930-chr7:100471250..100474138,3	MCF-7	breast:
39	chr7:100016949..100019484-chr7:100023454..100025888,2	MCF-7	breast:
40	chr7:99679133..99681399-chr7:100023910..100026674,3	K562	blood:
41	chr7:99035477..99037165-chr7:100025272..100027414,2	K562	blood:
42	chr7:100024499..100027894-chr7:100208680..100211740,5	MCF-7	breast:
43	chr7:99954086..99956374-chr7:100025281..100027347,2	MCF-7	breast:
44	chr7:100024516..100026521-chr7:100183469..100186366,2	MCF-7	breast:
45	chr7:100019883..100022700-chr7:100024204..100025806,2	MCF-7	breast:
46	chr7:100022010..100030260-chr7:100068697..100082544,31	K562	blood:
47	chr7:100024997..100029018-chr7:100182448..100185836,5	MCF-7	breast:
48	chr7:100024456..100030636-chr7:100180698..100187996,13	K562	blood:
49	chr7:100025085..100028095-chr7:100886628..100889556,3	MCF-7	breast:
50	chr7:99697112..99700279-chr7:100024243..100028129,6	MCF-7	breast:

No data

Variant related genes	Relation type
MEPCE	TF binding region
ENSG00000085514	Chromatin interaction
ENSG00000106290	Chromatin interaction
ENSG00000166924	Chromatin interaction
ENSG00000184414	Chromatin interaction
ENSG00000176125	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000146833	Chromatin interaction
ENSG00000201801	Chromatin interaction
ENSG00000106336	Chromatin interaction
ENSG00000121716	Chromatin interaction
ENSG00000166508	Chromatin interaction
ENSG00000224729	Chromatin interaction
ENSG00000214253	Chromatin interaction
ENSG00000172354	Chromatin interaction
ENSG00000266372	Chromatin interaction
ENSG00000106333	Chromatin interaction
ENSG00000166925	Chromatin interaction
ENSG00000106327	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000169871	Chromatin interaction
ENSG00000106246	Chromatin interaction
ENSG00000160917	Chromatin interaction
ENSG00000146830	Chromatin interaction
ENSG00000221838	Chromatin interaction
ENSG00000146826	Chromatin interaction
ENSG00000106330	Chromatin interaction
ENSG00000005483	Chromatin interaction
ENSG00000239569	Chromatin interaction
ENSG00000228393	Chromatin interaction
ENSG00000166526	Chromatin interaction
ENSG00000199347	Chromatin interaction
ENSG00000172336	Chromatin interaction
ENSG00000214309	Chromatin interaction
ENSG00000266154	Chromatin interaction
ENSG00000198498	Chromatin interaction
ENSG00000242798	Chromatin interaction
ENSG00000166997	Chromatin interaction
ENSG00000087087	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350965	chr7:99747460-100146105	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
2	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
3	nsv831071	chr7:99918025-100113413	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	287 gene(s)	inside rSNPs	diseases
4	nsv527107	chr7:100014711-100064719	Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	269 gene(s)	inside rSNPs	diseases
5	nsv888776	chr7:100014711-100198386	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	297 gene(s)	inside rSNPs	diseases
6	nsv888777	chr7:100014711-100221867	Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
7	nsv888778	chr7:100014711-100236593	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	310 gene(s)	inside rSNPs	diseases
8	nsv888779	chr7:100014711-100313420	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	321 gene(s)	inside rSNPs	diseases
9	esv3329388	chr7:100023441-100025989	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	88 gene(s)	inside rSNPs	diseases
10	esv3330521	chr7:100023666-100025889	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	72 gene(s)	inside rSNPs	diseases
11	esv3340427	chr7:100024116-100025464	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99987800-100025400	Weak transcription	Right Ventricle	heart
2	chr7:99995000-100025400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr7:99995000-100026000	Weak transcription	Primary T cells from cord blood	blood
4	chr7:99996200-100025400	Weak transcription	Brain Substantia Nigra	brain
5	chr7:99997400-100025600	Weak transcription	Aorta	Aorta
6	chr7:99998800-100025400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr7:99999000-100025400	Weak transcription	Left Ventricle	heart
8	chr7:99999400-100025400	Weak transcription	Psoas Muscle	Psoas
9	chr7:100000200-100025400	Weak transcription	Liver	Liver
10	chr7:100002800-100025400	Weak transcription	Brain Anterior Caudate	brain
11	chr7:100011600-100026000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr7:100011800-100025400	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr7:100011800-100025400	Weak transcription	Primary B cells from cord blood	blood
14	chr7:100011800-100025400	Weak transcription	Primary B cells from peripheral blood	blood
15	chr7:100011800-100025400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr7:100015000-100025400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr7:100015000-100025400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr7:100017000-100025400	Weak transcription	Brain Angular Gyrus	brain
19	chr7:100017400-100025400	Weak transcription	Brain Hippocampus Middle	brain
20	chr7:100017600-100025600	Weak transcription	Duodenum Mucosa	Duodenum
21	chr7:100017800-100025400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:100017800-100025400	Weak transcription	Adipose Nuclei	Adipose
23	chr7:100017800-100025600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr7:100018000-100025400	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr7:100018200-100025400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr7:100019000-100025400	Weak transcription	Fetal Brain Male	brain
27	chr7:100019200-100025400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:100019600-100025400	Weak transcription	HSMMtube	muscle
29	chr7:100020400-100025600	Weak transcription	Fetal Lung	lung
30	chr7:100020600-100025400	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr7:100020600-100025400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr7:100021000-100025400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:100021200-100025400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr7:100022000-100025400	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr7:100022000-100025400	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr7:100022200-100025600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:100023200-100025400	Weak transcription	GM12878-XiMat	blood
38	chr7:100024600-100025600	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr7:100024800-100025600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr7:100024800-100025600	Enhancers	Primary T cells fromperipheralblood	blood
41	chr7:100024800-100025600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr7:100024800-100025600	Weak transcription	HSMM	muscle
43	chr7:100025000-100025400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr7:100025200-100025400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr7:100025200-100025400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr7:100025200-100025400	Enhancers	Colon Smooth Muscle	Colon
47	chr7:100025200-100025400	Enhancers	Fetal Heart	heart
48	chr7:100025200-100025400	Enhancers	Placenta	Placenta
49	chr7:100025200-100025400	Enhancers	Stomach Smooth Muscle	stomach
50	chr7:100025200-100025400	Enhancers	A549	lung

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