Variant report

Variant	rs369158105
Chromosome Location	chr19:55865923-55865924
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr19:55864700-55866015	K562	blood:	n/a	chr19:55865340-55865350
2	CBX3	chr19:55865670-55865987	K562	blood:	n/a	n/a
3	SP1	chr19:55864929-55865951	A549	lung:	n/a	chr19:55865382-55865394 chr19:55865428-55865439 chr19:55865383-55865392 chr19:55865362-55865372 chr19:55865428-55865440 chr19:55865339-55865351 chr19:55865157-55865171 chr19:55865458-55865469 chr19:55865382-55865394 chr19:55865362-55865372 chr19:55865429-55865443
4	E2F6	chr19:55865597-55866022	K562	blood:	n/a	chr19:55865945-55865959
5	HEY1	chr19:55865695-55865949	K562	blood:	n/a	n/a
6	CTCF	chr19:55865895-55865927	GM12891	blood:	n/a	n/a
7	ZBTB7A	chr19:55865225-55866512	K562	blood:	n/a	chr19:55865945-55865954
8	POLR2A	chr19:55865567-55865949	K562	blood:	n/a	n/a
9	SP1	chr19:55865012-55865980	A549	lung:	n/a	chr19:55865382-55865394 chr19:55865428-55865439 chr19:55865383-55865392 chr19:55865362-55865372 chr19:55865428-55865440 chr19:55865339-55865351 chr19:55865157-55865171 chr19:55865458-55865469 chr19:55865382-55865394 chr19:55865362-55865372 chr19:55865429-55865443
10	CTCF	chr19:55865800-55865950	AG04449	skin:	n/a	n/a
11	POLR2A	chr19:55865681-55865959	MCF-7	breast:	n/a	n/a
12	POLR2A	chr19:55865178-55865967	K562	blood:	n/a	n/a
13	POLR2A	chr19:55865145-55865952	K562	blood:	n/a	n/a
14	POLR2A	chr19:55865707-55865937	MCF-7	breast:	n/a	n/a
15	UBTF	chr19:55865920-55865936	K562	blood:	n/a	n/a
16	MAX	chr19:55864874-55865949	A549	lung:	n/a	chr19:55865340-55865350
17	E2F6	chr19:55864933-55865933	A549	lung:	n/a	chr19:55865340-55865349
18	HMGN3	chr19:55865133-55866194	K562	blood:	n/a	n/a
19	ELF1	chr19:55865640-55866039	K562	blood:	n/a	n/a
20	ELF1	chr19:55865653-55866085	GM12878	blood:	n/a	n/a
21	BACH1	chr19:55865703-55866205	H1-hESC	embryonic stem cell:	n/a	n/a
22	ZBTB7A	chr19:55865547-55866468	ECC-1	luminal epithelium:	n/a	chr19:55865945-55865954
23	NFYB	chr19:55865919-55866305	K562	blood:	n/a	chr19:55866154-55866168 chr19:55866153-55866165 chr19:55866156-55866166 chr19:55866154-55866169 chr19:55866154-55866169
24	MAZ	chr19:55865196-55866025	K562	blood:	n/a	chr19:55865340-55865350
25	SIN3AK20	chr19:55865525-55866042	PANC-1	pancreas:	n/a	n/a
26	CTCF	chr19:55865887-55865987	NHEK	skin:	n/a	n/a
27	ZBTB7A	chr19:55865387-55865992	K562	blood:	n/a	chr19:55865945-55865954
28	ZBTB7A	chr19:55865096-55866547	ECC-1	luminal epithelium:	n/a	chr19:55865212-55865221 chr19:55865945-55865954

No.	Distal block	Cell Line	Cell type
1	chr19:55864929..55868342-chr19:55869494..55871064,3	MCF-7	breast:
2	chr19:55865530..55867437-chr19:55869222..55871050,2	K562	blood:
3	chr19:55725474..55728358-chr19:55864550..55866958,2	K562	blood:
4	chr19:55863699..55867009-chr19:55895864..55899065,4	MCF-7	breast:
5	chr19:55864955..55867658-chr19:55880222..55883231,3	MCF-7	breast:
6	chr19:55865626..55867203-chr19:55869204..55871320,2	K562	blood:
7	chr19:55864065..55867080-chr19:55895058..55897568,4	K562	blood:
8	chr19:55865908..55868131-chr19:55880960..55883611,2	MCF-7	breast:
9	chr19:55865213..55868465-chr19:55868824..55871801,4	MCF-7	breast:
10	chr19:55864307..55867114-chr19:56165229..56167152,3	K562	blood:
11	chr19:55726786..55728358-chr19:55864550..55866363,2	K562	blood:
12	chr19:55862642..55868480-chr19:55895176..55899926,10	K562	blood:
13	chr19:55865425..55868489-chr19:55917598..55920755,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM71E2-1	chr19:55865508-55866055	NONHSAT068029

Variant related genes	Relation type
COX6B2	TF binding region
ENSG00000233493	Chromatin interaction
ENSG00000267649	Chromatin interaction
ENSG00000095752	Chromatin interaction
ENSG00000108106	Chromatin interaction
ENSG00000063244	Chromatin interaction
ENSG00000108107	Chromatin interaction
ENSG00000267706	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1816335	chr19:55683977-55901099	Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv1065760	chr19:55721521-55929740	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
3	nsv912455	chr19:55725410-55879872	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
4	nsv912456	chr19:55725410-55925500	Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' 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	212 gene(s)	inside rSNPs	diseases
5	nsv912457	chr19:55725410-56019597	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	228 gene(s)	inside rSNPs	diseases
6	nsv432086	chr19:55807586-56050844	Weak transcription Bivalent Enhancer Genic enhancers Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	220 gene(s)	inside rSNPs	diseases
7	nsv912460	chr19:55814881-55897327	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
8	nsv912461	chr19:55845386-55897327	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
9	nsv470162	chr19:55845386-55902257	Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
10	nsv912462	chr19:55845386-55925500	Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	203 gene(s)	inside rSNPs	diseases
11	nsv912463	chr19:55845386-56004901	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers 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	219 gene(s)	inside rSNPs	diseases
12	nsv912464	chr19:55850269-55921164	Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	203 gene(s)	inside rSNPs	diseases
13	esv1799638	chr19:55850652-55883879	Weak transcription Strong transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
14	nsv516199	chr19:55854313-55901099	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
15	nsv912465	chr19:55854313-55935184	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
16	esv3430654	chr19:55864590-55867488	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
17	esv3405241	chr19:55865165-55868013	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:55864400-55866000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr19:55864400-55866000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr19:55864400-55866200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
4	chr19:55864600-55866000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
5	chr19:55864600-55866200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
6	chr19:55864600-55866200	Enhancers	Lung	lung
7	chr19:55864600-55866400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr19:55864800-55866000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
9	chr19:55864800-55866000	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr19:55864800-55866000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
11	chr19:55864800-55866000	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
12	chr19:55864800-55866000	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
13	chr19:55864800-55866000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr19:55864800-55866000	Flanking Bivalent TSS/Enh	Thymus	Thymus
15	chr19:55864800-55866000	Flanking Active TSS	HMEC	breast
16	chr19:55864800-55866000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
17	chr19:55864800-55866200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
18	chr19:55864800-55866200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr19:55864800-55866400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
20	chr19:55864800-55866800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
21	chr19:55865000-55866000	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr19:55865000-55866000	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
23	chr19:55865000-55866000	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood
24	chr19:55865000-55866200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
25	chr19:55865000-55866200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
26	chr19:55865000-55866400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
27	chr19:55865000-55866400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr19:55865000-55866400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr19:55865200-55866000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
30	chr19:55865200-55866000	Active TSS	Duodenum Mucosa	Duodenum
31	chr19:55865200-55866000	Bivalent Enhancer	Fetal Brain Male	brain
32	chr19:55865200-55866000	Enhancers	Fetal Heart	heart
33	chr19:55865200-55866000	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
34	chr19:55865200-55866000	Active TSS	K562	blood
35	chr19:55865200-55866200	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr19:55865200-55866200	Bivalent/Poised TSS	A549	lung
37	chr19:55865200-55866800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
38	chr19:55865400-55866000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr19:55865400-55866000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
40	chr19:55865400-55866000	Bivalent/Poised TSS	Esophagus	oesophagus
41	chr19:55865400-55866200	Bivalent/Poised TSS	Primary neutrophils fromperipheralblood	blood
42	chr19:55865400-55866200	Bivalent/Poised TSS	HepG2	liver
43	chr19:55865400-55866400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr19:55865400-55866400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr19:55865400-55867000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr19:55865600-55866000	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr19:55865600-55866000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
48	chr19:55865600-55866000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr19:55865600-55866000	Bivalent Enhancer	Fetal Intestine Large	intestine
50	chr19:55865600-55866200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood

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