Variant report

Variant	nsv822520
Chromosome Location	chr1:46650486-46661701
allele	n/a
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	CCNT2	chr1:46651021-46651285	K562	blood:	n/a	n/a
2	CEBPB	chr1:46661155-46661378	HepG2	liver:	n/a	chr1:46661307-46661318
3	CEBPB	chr1:46661253-46661340	K562	blood:	n/a	chr1:46661307-46661318
4	CTCF	chr1:46654120-46654270	AG10803	skin:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
5	CTCF	chr1:46654160-46654310	NHDF-neo	bronchial:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
6	CTCF	chr1:46654120-46654270	HA-sp	spinal cord:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
7	CTCF	chr1:46654084-46654371	K562	blood:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
8	CTCF	chr1:46654140-46654290	SAEC	small airway:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
9	CTCF	chr1:46654140-46654290	NHEK	skin:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
10	CTCF	chr1:46654140-46654290	HPAF	blood vessel:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
11	CTCF	chr1:46654201-46654245	GM12878	blood:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
12	CTCF	chr1:46654100-46654250	HEEpiC	esophagus:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
13	CTCF	chr1:46654160-46654310	K562	blood:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
14	CTCF	chr1:46654022-46654401	MCF-7	breast:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
15	CTCF	chr1:46654180-46654330	BE2_C	brain:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
16	CTCF	chr1:46654260-46654410	HCFaa	heart:	n/a	n/a
17	CTCF	chr1:46654180-46654330	HUVEC	blood vessel:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
18	CTCF	chr1:46654100-46654250	RPTEC	kidney:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
19	CTCF	chr1:46654169-46654259	GM10266	blood:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
20	CTCF	chr1:46654181-46654234	GM19238	blood:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
21	CTCF	chr1:46654200-46654350	HFF	foreskin:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
22	CTCF	chr1:46654147-46654239	MCF-7	breast:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
23	CTCF	chr1:46654140-46654290	HEEpiC	esophagus:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
24	CTCF	chr1:46654111-46654325	MCF-7	breast:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
25	CTCF	chr1:46654120-46654270	HepG2	liver:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
26	CTCF	chr1:46654120-46654270	HCT-116	colon:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
27	CTCF	chr1:46654160-46654310	AG09319	gingival:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
28	CTCF	chr1:46654133-46654311	MCF-7	breast:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
29	CTCF	chr1:46654229-46654244	HepG2	liver:	n/a	n/a
30	CTCF	chr1:46654020-46654170	BJ	skin:	n/a	n/a
31	CTCF	chr1:46654080-46654230	HA-sp	spinal cord:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
32	CTCF	chr1:46654180-46654330	BJ	skin:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
33	CTCF	chr1:46654140-46654290	SK-N-SH_RA	brain:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
34	CTCF	chr1:46654198-46654276	ProgFib	skin:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
35	CTCF	chr1:46654140-46654290	AG04449	skin:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
36	CTCF	chr1:46654190-46654257	GM12878	blood:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
37	CTCF	chr1:46654160-46654310	HMEC	breast:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
38	CTCF	chr1:46654120-46654270	HCPEpiC	choroid plexus:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
39	CTCF	chr1:46654065-46654281	K562	blood:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
40	CTCF	chr1:46654142-46654296	NHEK	skin:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
41	CTCF	chr1:46654140-46654290	GM12878	blood:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
42	CTCF	chr1:46654160-46654310	Caco-2	colon:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
43	CTCF	chr1:46654140-46654290	HMF	breast:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
44	CTCF	chr1:46651260-46651410	GM12865	blood:	n/a	n/a
45	CTCF	chr1:46654100-46654250	NHDF-neo	bronchial:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
46	CTCF	chr1:46654180-46654330	HAc	cerebellar:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
47	CTCF	chr1:46654060-46654210	HCFaa	heart:	n/a	n/a
48	CTCF	chr1:46654100-46654250	MCF-7	breast:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
49	CTCF	chr1:46654146-46654301	HepG2	liver:	n/a	chr1:46654214-46654223 chr1:46654208-46654226
50	CTCF	chr1:46654180-46654330	AG10803	skin:	n/a	chr1:46654214-46654223 chr1:46654208-46654226

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:46657852-46657902	MCF10A-Er-Src	breast:	n/a
2	chr1:46654770-46654820	A549	lung:	n/a
3	chr1:46651377-46651427	RPTEC	kidney:	n/a
4	chr1:46657852-46657902	GM19239	blood:	n/a
5	chr1:46651377-46651427	SK-N-SH_RA	brain:	n/a
6	chr1:46657852-46657902	AG09319	gingival:	n/a
7	chr1:46657852-46657902	CMK	blood:	n/a
8	chr1:46657852-46657902	HPAEpiC	pulmonary alveolar:	n/a
9	chr1:46651377-46651427	GM06990	blood:	n/a
10	chr1:46657852-46657902	HRE	kidney:	n/a
11	chr1:46657852-46657902	HRCEpiC	kidney:	n/a
12	chr1:46651377-46651427	HEEpiC	esophagus:	n/a
13	chr1:46657852-46657902	HEK293	kidney:	embryo
14	chr1:46657852-46657902	U87	brain:	n/a
15	chr1:46651377-46651427	GM12892	blood:	n/a
16	chr1:46654770-46654820	NHDF-neo	bronchial:	n/a
17	chr1:46651377-46651427	GM12891	blood:	n/a
18	chr1:46657852-46657902	AG04450	lung:	fetal
19	chr1:46657852-46657902	SK-N-SH_RA	brain:	n/a
20	chr1:46657852-46657902	GM06990	blood:	n/a
21	chr1:46657852-46657902	ProgFib	skin:	n/a
22	chr1:46654770-46654820	AG04449	skin:	fetal
23	chr1:46654770-46654820	MCF-7	breast:	n/a
24	chr1:46654770-46654820	SK-N-SH_RA	brain:	n/a
25	chr1:46651377-46651427	NH-A	brain:	n/a
26	chr1:46657852-46657902	HIPEpiC	eye:	n/a
27	chr1:46651377-46651427	GM19239	blood:	n/a
28	chr1:46654770-46654820	BE2_C	brain:	n/a
29	chr1:46651377-46651427	AG09319	gingival:	n/a
30	chr1:46657852-46657902	AG10803	skin:	n/a
31	chr1:46651377-46651427	T-47D	breast:	n/a
32	chr1:46651377-46651427	HNPCEpiC	eye:	n/a
33	chr1:46651377-46651427	HUVEC	blood vessel:	n/a
34	chr1:46654770-46654820	Caco-2	colon:	n/a
35	chr1:46657852-46657902	SAEC	small airway:	n/a
36	chr1:46651377-46651427	HCT-116	colon:	n/a
37	chr1:46651377-46651427	HAEpiC	amniotic membrane:	n/a
38	chr1:46657852-46657902	BE2_C	brain:	n/a
39	chr1:46654770-46654820	GM12892	blood:	n/a
40	chr1:46657852-46657902	HCF	heart:	n/a
41	chr1:46657852-46657902	NHDF-neo	bronchial:	n/a
42	chr1:46651377-46651427	HIPEpiC	eye:	n/a
43	chr1:46654770-46654820	HepG2	liver:	n/a
44	chr1:46657852-46657902	IMR90	lung:	fetal
45	chr1:46651377-46651427	PFSK-1	brain:	n/a
46	chr1:46657852-46657902	HCM	heart:	n/a
47	chr1:46651377-46651427	AG04449	skin:	fetal
48	chr1:46654770-46654820	IMR90	lung:	fetal
49	chr1:46651377-46651427	ProgFib	skin:	n/a
50	chr1:46651377-46651427	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:46649178..46652657-chr1:46804646..46808340,3	K562	blood:
2	chr1:46506035..46508905-chr1:46652917..46655021,2	K562	blood:
3	chr1:46593944..46606364-chr1:46632700..46654752,92	MCF-7	breast:
4	chr1:46650088..46654431-chr1:46660649..46664517,6	K562	blood:
5	chr1:46654141..46655065-chr1:46686530..46687520,2	K562	blood:
6	chr1:46649532..46653630-chr1:46654229..46657626,5	K562	blood:
7	chr1:46650088..46654431-chr1:46660649..46664517,6	K562	blood:
8	chr1:46635707..46641847-chr1:46658318..46665376,6	K562	blood:
9	chr1:46651145..46653630-chr1:46655330..46656931,2	K562	blood:
10	chr1:46511398..46513219-chr1:46661327..46664273,2	K562	blood:
11	chr1:46655055..46657089-chr1:46660315..46664109,3	K562	blood:
12	chr1:46592691..46601867-chr1:46642778..46650670,25	MCF-7	breast:
13	chr1:46655107..46657515-chr1:46657628..46660092,2	K562	blood:
14	chr1:46645973..46650649-chr1:46685566..46691437,5	MCF-7	breast:
15	chr1:46649532..46653630-chr1:46654229..46657626,5	K562	blood:
16	chr1:46597572..46599707-chr1:46650898..46652531,2	K562	blood:
17	chr1:46655107..46657515-chr1:46657628..46660092,2	K562	blood:
18	chr1:46636697..46639165-chr1:46652056..46653716,2	MCF-7	breast:
19	chr1:46655055..46657089-chr1:46660315..46664109,3	K562	blood:
20	chr1:46597522..46599871-chr1:46652331..46654981,2	MCF-7	breast:
21	chr1:46635040..46637380-chr1:46652840..46654559,2	MCF-7	breast:
22	chr1:46595304..46602065-chr1:46660247..46665309,8	MCF-7	breast:
23	chr1:46641730..46644233-chr1:46656558..46658079,2	K562	blood:
24	chr1:46648447..46653398-chr1:46660649..46666552,10	K562	blood:
25	chr1:46648447..46653398-chr1:46660649..46666552,10	K562	blood:
26	chr1:46596990..46600235-chr1:46653510..46656266,3	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location
1	POMGNT1	hsa-miR-103a-3p	chr1:46656605-46656628
2	POMGNT1	hsa-miR-103a-3p	chr1:46654553-46654575
3	POMGNT1	hsa-miR-330-5p	chr1:46656879-46656900

Variant related genes	Relation type
TSPAN1	TF binding region
POMGNT1	TF binding region
TSPAN1	CpG island
POMGNT1	CpG island
ENSG00000117481	chromatin interactions
ENSG00000227857	chromatin interactions
ENSG00000117472	chromatin interactions
ENSG00000117461	chromatin interactions
ENSG00000250719	chromatin interactions
ENSG00000085998	chromatin interactions
ENSG00000226957	chromatin interactions

Extended variants
information (count: 526 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540727697	chr1:46650515-46650516	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs41286815	chr1:46650542-46650543	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs374613620	chr1:46650561-46650562	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs111543379	chr1:46650658-46650659	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs201800369	chr1:46650660-46650661	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs146559665	chr1:46650661-46650662	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs564474415	chr1:46650697-46650698	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs370460447	chr1:46650728-46650729	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs557697693	chr1:46650733-46650734	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs1047216	chr1:46650758-46650759	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs201547396	chr1:46650763-46650764	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs200479864	chr1:46650773-46650774	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs530826356	chr1:46650789-46650790	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs543042784	chr1:46650824-46650825	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs374820445	chr1:46650827-46650828	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs112401991	chr1:46650839-46650840	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs2234271	chr1:46650842-46650843	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs571878133	chr1:46650849-46650850	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs56335143	chr1:46650866-46650867	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs368041262	chr1:46650872-46650873	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs370368119	chr1:46650901-46650902	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs144913574	chr1:46650921-46650922	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs375232447	chr1:46650928-46650929	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs368462173	chr1:46650944-46650945	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs149302587	chr1:46650945-46650946	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs200863715	chr1:46650965-46650966	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs371861627	chr1:46650978-46650979	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs375561647	chr1:46650988-46650989	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs147317474	chr1:46651049-46651050	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs2234272	chr1:46651082-46651083	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs554994359	chr1:46651089-46651090	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs368597879	chr1:46651118-46651119	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs371341960	chr1:46651119-46651120	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs374769507	chr1:46651128-46651129	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs371609599	chr1:46651131-46651132	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs566915171	chr1:46651132-46651133	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs34463133	chr1:46651169-46651170	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs376073263	chr1:46651181-46651182	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs552603653	chr1:46651196-46651197	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs147137223	chr1:46651202-46651203	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs199685801	chr1:46651222-46651223	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs201843939	chr1:46651255-46651256	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs112015052	chr1:46651258-46651259	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs1802371	chr1:46651296-46651297	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs373512282	chr1:46651341-46651342	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs556863534	chr1:46651369-46651370	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs575522016	chr1:46651397-46651398	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs542554576	chr1:46651412-46651413	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs1802372	chr1:46651452-46651453	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs1802309	chr1:46651478-46651479	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	19287155	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Neuroblastoma	21899760	CNVD
Uveal melanoma	20484589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46639400-46653800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:46639600-46652800	Weak transcription	Brain Germinal Matrix	brain
3	chr1:46640800-46656400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:46644800-46651400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr1:46645000-46651400	Enhancers	Fetal Thymus	thymus
6	chr1:46645200-46651400	Enhancers	Pancreas	Pancrea
7	chr1:46645200-46657800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr1:46645400-46650600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr1:46645400-46652200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:46645600-46650800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr1:46645600-46652800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr1:46645600-46653200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr1:46645600-46653600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr1:46645600-46658200	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr1:46645800-46663200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr1:46646000-46652800	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr1:46646000-46653200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr1:46646000-46654400	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr1:46646000-46657600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr1:46646200-46650800	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr1:46646200-46652800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:46646400-46650800	Weak transcription	Brain Cingulate Gyrus	brain
23	chr1:46647000-46650600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:46647000-46651400	Enhancers	Muscle Satellite Cultured Cells	--
25	chr1:46647000-46653400	Weak transcription	Fetal Brain Male	brain
26	chr1:46647200-46651400	Enhancers	HSMM	muscle
27	chr1:46647200-46653000	Weak transcription	Fetal Brain Female	brain
28	chr1:46647400-46651600	Enhancers	Spleen	Spleen
29	chr1:46648000-46653000	Weak transcription	Dnd41	blood
30	chr1:46648200-46650600	Enhancers	Duodenum Mucosa	Duodenum
31	chr1:46648400-46651000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:46648400-46652200	Enhancers	Left Ventricle	heart
33	chr1:46648400-46657800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr1:46648600-46653400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr1:46648800-46650600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:46648800-46650600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:46648800-46651000	Enhancers	Lung	lung
38	chr1:46648800-46651400	Enhancers	HSMMtube	muscle
39	chr1:46648800-46651600	Enhancers	Right Ventricle	heart
40	chr1:46648800-46653000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr1:46649000-46651200	Enhancers	GM12878-XiMat	blood
42	chr1:46649000-46652800	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr1:46649200-46650600	Weak transcription	Stomach Smooth Muscle	stomach
44	chr1:46649200-46651000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr1:46649200-46651000	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr1:46649200-46651000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr1:46649200-46651400	Enhancers	Thymus	Thymus
48	chr1:46649200-46651600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr1:46649200-46652200	Enhancers	Esophagus	oesophagus
50	chr1:46649200-46652800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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