Variant report

Variant	rs374160203
Chromosome Location	chr21:44596543-44596544
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:44595103..44597994-chr21:45059971..45061669,2	MCF-7	breast:
2	chr21:44595418..44598407-chr21:45007465..45009708,2	MCF-7	breast:
3	chr21:44595798..44598770-chr21:45063265..45067849,4	MCF-7	breast:
4	chr21:44596001..44597609-chr21:45065167..45067189,15	MCF-7	breast:
5	chr21:44595907..44598227-chr21:44599190..44600855,2	MCF-7	breast:
6	chr21:44596450..44597355-chr21:44683459..44684057,2	MCF-7	breast:
7	chr21:44595975..44600241-chr21:44843202..44849395,11	MCF-7	breast:
8	chr21:44596467..44597366-chr21:45066269..45067210,6	K562	blood:
9	chr21:44594966..44597591-chr21:44845721..44847643,2	K562	blood:
10	chr21:44595827..44599164-chr21:44845631..44847666,4	MCF-7	breast:
11	chr21:44595581..44597977-chr21:44722947..44725523,2	K562	blood:
12	chr21:44558793..44559748-chr21:44595983..44597245,4	MCF-7	breast:
13	chr21:44596302..44600320-chr21:44763162..44765941,4	MCF-7	breast:
14	chr21:44595496..44597017-chr21:44829022..44831353,2	MCF-7	breast:
15	chr21:44596413..44596968-chr21:44866121..44867152,3	K562	blood:
16	chr21:44596497..44597381-chr21:44847015..44847854,5	K562	blood:
17	chr21:44596396..44597313-chr21:45065147..45065707,2	MCF-7	breast:
18	chr21:44596361..44597517-chr21:45066264..45067091,4	MCF-7	breast:
19	chr21:44596524..44597433-chr21:45039423..45039934,2	K562	blood:
20	chr21:44596483..44597010-chr21:44689136..44690000,2	K562	blood:
21	chr21:44596353..44597867-chr21:44760877..44763023,2	MCF-7	breast:
22	chr21:44595506..44597559-chr21:44837131..44839693,2	MCF-7	breast:
23	chr21:44582210..44584160-chr21:44594583..44597207,2	MCF-7	breast:
24	chr21:44595703..44598660-chr21:45028207..45031192,2	MCF-7	breast:
25	chr21:44558924..44559647-chr21:44596413..44597304,3	MCF-7	breast:
26	chr21:44588285..44592993-chr21:44594253..44598657,5	MCF-7	breast:
27	chr21:44594665..44597116-chr21:44751236..44753866,2	MCF-7	breast:
28	chr21:44596408..44597544-chr21:44922093..44923863,11	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000142178	Chromatin interaction
ENSG00000228120	Chromatin interaction
ENSG00000237864	Chromatin interaction
ENSG00000188660	Chromatin interaction
ENSG00000160202	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv913812	chr21:44213057-44686358	Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	esv1827985	chr21:44447198-44596778	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv913828	chr21:44471692-44598827	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv1067412	chr21:44526656-44772130	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
5	nsv1056684	chr21:44539714-44886119	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
6	nsv1060276	chr21:44550394-44628579	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv913831	chr21:44563995-44931821	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
8	nsv913832	chr21:44579105-44768562	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv587664	chr21:44585405-44598827	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
10	esv3440728	chr21:44595883-44600181	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:44586200-44597000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr21:44590200-44596600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr21:44592400-44596800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr21:44593600-44596600	Enhancers	Brain Germinal Matrix	brain
5	chr21:44593600-44597000	Weak transcription	Psoas Muscle	Psoas
6	chr21:44593800-44596600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr21:44593800-44596600	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr21:44593800-44596600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr21:44593800-44596600	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr21:44593800-44596600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr21:44593800-44596600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr21:44593800-44596600	Weak transcription	Liver	Liver
13	chr21:44593800-44596600	Weak transcription	Left Ventricle	heart
14	chr21:44593800-44596600	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr21:44593800-44596600	Weak transcription	Right Atrium	heart
16	chr21:44593800-44596800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr21:44593800-44596800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr21:44593800-44596800	Enhancers	Fetal Thymus	thymus
19	chr21:44593800-44597000	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr21:44593800-44597000	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr21:44593800-44597000	Weak transcription	Primary hematopoietic stem cells	blood
22	chr21:44593800-44597000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr21:44593800-44599000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr21:44593800-44599800	Enhancers	Placenta	Placenta
25	chr21:44593800-44601600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr21:44594000-44596600	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr21:44594000-44596600	Weak transcription	Primary B cells from cord blood	blood
28	chr21:44594000-44596600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr21:44594000-44596600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr21:44594000-44596600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr21:44594000-44596600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr21:44594000-44596600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr21:44594000-44596600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr21:44594000-44596600	Weak transcription	Brain Substantia Nigra	brain
35	chr21:44594000-44596600	Weak transcription	Esophagus	oesophagus
36	chr21:44594000-44596600	Weak transcription	Fetal Lung	lung
37	chr21:44594000-44596600	Enhancers	HepG2	liver
38	chr21:44594000-44596600	Weak transcription	HSMM	muscle
39	chr21:44594000-44596600	Weak transcription	NH-A	brain
40	chr21:44594000-44596800	Weak transcription	Primary T cells from cord blood	blood
41	chr21:44594000-44596800	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr21:44594000-44597000	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr21:44594000-44597000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr21:44594000-44597000	Weak transcription	Lung	lung
45	chr21:44594000-44597000	Weak transcription	Right Ventricle	heart
46	chr21:44594000-44597000	Weak transcription	NHDF-Ad	bronchial
47	chr21:44594000-44597400	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr21:44594000-44598200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr21:44594200-44597000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr21:44594400-44597000	Weak transcription	Gastric	stomach

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