Variant report

Variant	rs553867787
Chromosome Location	chr7:27138849-27138850
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:18)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:18 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SP1	chr7:27138777-27139587	H1-hESC	embryonic stem cell:	n/a	n/a
2	SIN3AK20	chr7:27137647-27139006	PANC-1	pancreas:	n/a	n/a
3	POLR2A	chr7:27137526-27139036	HUVEC	blood vessel:	n/a	n/a
4	TCF7L2	chr7:27137605-27139062	PANC-1	pancreas:	n/a	n/a
5	TBP	chr7:27138658-27138849	H1-hESC	embryonic stem cell:	n/a	n/a
6	POLR2A	chr7:27138103-27139000	HUVEC	blood vessel:	n/a	n/a
7	POLR2A	chr7:27135166-27139184	PANC-1	pancreas:	n/a	n/a
8	MYC	chr7:27138346-27139120	MCF10A-Er-Src	breast:	n/a	n/a
9	POLR2A	chr7:27135394-27139167	MCF10A-Er-Src	breast:	n/a	n/a
10	POLR2A	chr7:27137292-27139236	PANC-1	pancreas:	n/a	n/a
11	SIN3AK20	chr7:27138483-27138986	PANC-1	pancreas:	n/a	n/a
12	KAP1	chr7:27138737-27138977	HEK293	kidney:	n/a	n/a
13	POLR2A	chr7:27135386-27149832	IMR90	lung:	n/a	n/a
14	MYC	chr7:27138476-27139129	MCF10A-Er-Src	breast:	n/a	n/a
15	POLR2A	chr7:27138509-27139129	H1-neurons	neurons:	n/a	n/a
16	RAD21	chr7:27135269-27138922	IMR90	lung:	n/a	n/a
17	SUZ12	chr7:27137564-27139059	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr7:27134717-27152399	IMR90	lung:	n/a	chr7:27141647-27141657

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:27136545..27139680-chr7:27140711..27142949,3	K562	blood:
2	7:27137201-27143270..7:27162022-27164727	H1-hESC	embryonic stem cell:	embryo
3	chr7:27136703..27139680-chr7:27141228..27142949,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EVX1-13	chr7:27138717-27138985	ENSG00000233429.4
2	lnc-EVX1-13	chr7:27138717-27138985	ENSG00000233429.4
3	lnc-EVX1-13	chr7:27138458-27138985	ENSG00000233429.4
4	lnc-EVX1-13	chr7:27138458-27138985	ENSG00000233429.4
5	lnc-EVX1-13	chr7:27138693-27138985	ENSG00000233429.4
6	lnc-EVX1-13	chr7:27138693-27138985	ENSG00000233429.4
7	lnc-EVX1-13	chr7:27138717-27138985	NONHSAT119664

No data

Variant related genes	Relation type
HOXA1	TF binding region
HOTAIRM1	TF binding region
ENSG00000105996	Chromatin interaction
ENSG00000253552	Chromatin interaction
HOXA4	LncRNA region
HOXA1	LncRNA region

Extended variants
information (count: 29 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025538	chr7:26482342-27376045	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
2	nsv538805	chr7:26482342-27376045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
3	nsv1018709	chr7:26990384-27216552	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
4	nsv538806	chr7:26990384-27216552	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
5	nsv887856	chr7:27073731-27297791	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
6	nsv824038	chr7:27119294-27284522	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
7	nsv887857	chr7:27120689-27229549	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
8	nsv824039	chr7:27121825-27294951	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
9	nsv824040	chr7:27121870-27295010	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
10	nsv887858	chr7:27127231-27188659	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
11	nsv887860	chr7:27127231-27196069	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
12	nsv887859	chr7:27127231-27196113	Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
13	nsv887861	chr7:27127231-27206688	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
14	nsv887862	chr7:27127231-27217359	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
15	nsv887863	chr7:27127231-27243106	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
16	nsv887864	chr7:27127231-27243962	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
17	nsv887865	chr7:27127231-27247279	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
18	nsv887866	chr7:27127231-27248373	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
19	nsv887867	chr7:27127231-27252246	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
20	nsv824041	chr7:27128039-27294951	Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
21	nsv606463	chr7:27135314-27182245	Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
22	nsv887868	chr7:27135314-27202289	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
23	nsv887869	chr7:27135314-27297791	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
24	nsv887870	chr7:27136308-27154737	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
25	nsv887871	chr7:27136308-27179814	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
26	nsv887872	chr7:27136308-27181437	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
27	nsv887873	chr7:27136308-27186495	Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
28	nsv887874	chr7:27136308-27196069	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
29	nsv606464	chr7:27138478-27168590	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27134400-27139000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:27134400-27139000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:27134400-27139000	Active TSS	HMEC	breast
4	chr7:27134800-27139200	Bivalent/Poised TSS	NH-A	brain
5	chr7:27134800-27140200	Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr7:27135000-27139400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
7	chr7:27135200-27139000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
8	chr7:27135200-27139200	Active TSS	Aorta	Aorta
9	chr7:27135200-27139200	Active TSS	Right Atrium	heart
10	chr7:27135400-27139000	Active TSS	Esophagus	oesophagus
11	chr7:27136200-27139200	Flanking Active TSS	Adipose Nuclei	Adipose
12	chr7:27136800-27139000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
13	chr7:27136800-27139400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
14	chr7:27137000-27139000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
15	chr7:27137000-27139000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
16	chr7:27137000-27139000	Enhancers	Pancreas	Pancrea
17	chr7:27137000-27146800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr7:27137200-27139000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
19	chr7:27137200-27139600	Bivalent/Poised TSS	Fetal Lung	lung
20	chr7:27137400-27139800	Flanking Active TSS	HUVEC	blood vessel
21	chr7:27137400-27140600	Weak transcription	HSMMtube	muscle
22	chr7:27137400-27140800	Transcr. at gene 5' and 3'	NHEK	skin
23	chr7:27137600-27139200	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:27137600-27139400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
25	chr7:27137600-27149000	Weak transcription	HepG2	liver
26	chr7:27137800-27139000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:27137800-27139000	Active TSS	Lung	lung
28	chr7:27138000-27139000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr7:27138000-27139200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
30	chr7:27138000-27139200	Active TSS	Stomach Mucosa	stomach
31	chr7:27138000-27144200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr7:27138000-27144800	Weak transcription	A549	lung
33	chr7:27138200-27139000	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
34	chr7:27138200-27139000	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
35	chr7:27138200-27141600	Weak transcription	Spleen	Spleen
36	chr7:27138400-27139000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
37	chr7:27138400-27139000	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
38	chr7:27138400-27139000	Bivalent/Poised TSS	Thymus	Thymus
39	chr7:27138400-27139200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:27138400-27139200	Flanking Active TSS	Placenta Amnion	Placenta Amnion
41	chr7:27138400-27139400	Bivalent Enhancer	Liver	Liver
42	chr7:27138400-27140400	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr7:27138600-27139000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
44	chr7:27138600-27139000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
45	chr7:27138600-27139000	Bivalent/Poised TSS	Primary T cells from cord blood	blood
46	chr7:27138600-27139000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr7:27138600-27139000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr7:27138600-27139000	Flanking Active TSS	Colonic Mucosa	Colon
49	chr7:27138600-27139000	Bivalent Enhancer	Small Intestine	intestine
50	chr7:27138600-27139000	Transcr. at gene 5' and 3'	NHLF	lung

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