Variant report

Variant	rs138796805
Chromosome Location	chr19:18174634-18174635
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:18174502..18178222-chr19:18262412..18264976,3	K562	blood:
2	chr19:18173990..18174805-chr19:18278703..18279468,3	K562	blood:

Variant related genes	Relation type
ENSG00000268173	Chromatin interaction
ENSG00000105647	Chromatin interaction
ENSG00000269145	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055932	chr19:17923918-18369944	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
2	nsv543923	chr19:17923918-18369944	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
3	nsv532614	chr19:18033043-18573963	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
4	nsv470130	chr19:18047283-18234587	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
5	esv1837595	chr19:18085428-18393682	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
6	nsv911235	chr19:18143862-18175853	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	nsv833773	chr19:18152971-18302988	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
8	nsv578742	chr19:18168674-18181779	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
9	nsv911236	chr19:18169314-18175853	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
10	nsv911237	chr19:18169449-18193060	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
11	nsv911238	chr19:18172004-18180194	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
12	nsv578743	chr19:18172841-18179973	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
13	nsv911239	chr19:18173603-18191059	Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
14	nsv1067871	chr19:18174031-18186197	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18169200-18190000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr19:18169600-18185600	Weak transcription	Esophagus	oesophagus
3	chr19:18169600-18195000	Weak transcription	Gastric	stomach
4	chr19:18169800-18175800	Weak transcription	Hela-S3	cervix
5	chr19:18169800-18178800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr19:18169800-18179600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr19:18169800-18180000	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr19:18169800-18180200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr19:18169800-18180200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr19:18169800-18181000	Weak transcription	Primary B cells from peripheral blood	blood
11	chr19:18169800-18181000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr19:18169800-18183000	Weak transcription	Thymus	Thymus
13	chr19:18169800-18183800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr19:18169800-18183800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr19:18169800-18185000	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr19:18170000-18178400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr19:18170000-18184000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr19:18170200-18181000	Weak transcription	Fetal Thymus	thymus
19	chr19:18170200-18184200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr19:18170200-18197000	Weak transcription	Primary B cells from cord blood	blood
21	chr19:18170400-18180800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr19:18170400-18184000	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr19:18171000-18183000	Weak transcription	GM12878-XiMat	blood
24	chr19:18171800-18180000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr19:18172000-18175600	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr19:18172000-18175800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr19:18173200-18179200	Weak transcription	Spleen	Spleen
28	chr19:18173200-18181000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr19:18174200-18177800	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr19:18174200-18180800	Strong transcription	Primary T cells from cord blood	blood
31	chr19:18174400-18176400	Enhancers	K562	blood

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