Variant report

Variant	nsv873243
Chromosome Location	chr1:227581017-227617519
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:348)
CpG islands
(count:61)
Chromatin interactive
region (count:39)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:227584166-227585575	K562	blood:	n/a	n/a
2	ATF1	chr1:227605599-227605829	K562	blood:	n/a	n/a
3	ATF1	chr1:227584145-227585205	K562	blood:	n/a	n/a
4	ATF3	chr1:227584112-227584882	K562	blood:	n/a	n/a
5	ATF3	chr1:227616337-227616828	A549	lung:	n/a	n/a
6	ATF3	chr1:227584139-227584421	K562	blood:	n/a	n/a
7	ATF3	chr1:227598778-227599031	K562	blood:	n/a	n/a
8	BACH1	chr1:227610762-227610765	K562	blood:	n/a	n/a
9	BCL3	chr1:227616353-227616868	A549	lung:	n/a	n/a
10	BCLAF1	chr1:227584121-227585083	K562	blood:	n/a	n/a
11	BHLHE40	chr1:227584180-227585308	K562	blood:	n/a	n/a
12	CBX3	chr1:227584085-227585332	K562	blood:	n/a	n/a
13	CBX3	chr1:227584104-227584693	K562	blood:	n/a	n/a
14	CBX3	chr1:227589248-227589617	K562	blood:	n/a	n/a
15	CCNT2	chr1:227584149-227584854	K562	blood:	n/a	n/a
16	CEBPB	chr1:227605650-227605911	K562	blood:	n/a	n/a
17	CEBPB	chr1:227602449-227602663	A549	lung:	n/a	n/a
18	CEBPB	chr1:227584223-227584866	K562	blood:	n/a	n/a
19	CEBPB	chr1:227584104-227585186	K562	blood:	n/a	n/a
20	CEBPB	chr1:227580902-227581351	K562	blood:	n/a	n/a
21	CEBPB	chr1:227617166-227617348	A549	lung:	n/a	n/a
22	CEBPB	chr1:227609030-227609278	K562	blood:	n/a	n/a
23	CEBPB	chr1:227598785-227599091	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:227602391-227602623	K562	blood:	n/a	n/a
25	CEBPB	chr1:227605599-227605990	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:227598870-227599069	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:227615190-227615851	A549	lung:	n/a	chr1:227615658-227615671
28	CEBPB	chr1:227615276-227615775	K562	blood:	n/a	chr1:227615658-227615671
29	CEBPB	chr1:227605714-227605810	A549	lung:	n/a	n/a
30	CEBPD	chr1:227584177-227585362	K562	blood:	n/a	n/a
31	CEBPD	chr1:227584014-227585311	K562	blood:	n/a	n/a
32	CHD2	chr1:227584219-227585146	K562	blood:	n/a	n/a
33	CREB1	chr1:227616546-227616899	A549	lung:	n/a	n/a
34	CREB1	chr1:227583997-227584981	K562	blood:	n/a	n/a
35	CREB1	chr1:227584152-227584684	K562	blood:	n/a	n/a
36	CTCF	chr1:227591755-227591804	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr1:227610060-227610210	AG09319	gingival:	n/a	n/a
38	CTCF	chr1:227611040-227611158	GM13976	blood:	n/a	n/a
39	CTCF	chr1:227583716-227583910	K562	blood:	n/a	n/a
40	CTCF	chr1:227612304-227612311	K562	blood:	n/a	n/a
41	CTCF	chr1:227609600-227609750	GM12869	blood:	n/a	n/a
42	CTCF	chr1:227582305-227582376	Lung_OC	lung:	n/a	n/a
43	CUX1	chr1:227583570-227583844	K562	blood:	n/a	n/a
44	CUX1	chr1:227617439-227618068	K562	blood:	n/a	n/a
45	CUX1	chr1:227584149-227585596	K562	blood:	n/a	n/a
46	E2F4	chr1:227605679-227605923	MCF10A-Er-Src	breast:	n/a	n/a
47	EBF1	chr1:227589680-227589892	GM12878	blood:	n/a	n/a
48	EBF1	chr1:227591271-227591504	GM12878	blood:	n/a	n/a
49	EBF1	chr1:227591302-227591552	GM12878	blood:	n/a	n/a
50	EGR1	chr1:227607806-227608218	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:227612340-227612390	GM19239	blood:	n/a
2	chr1:227612340-227612390	CMK	blood:	n/a
3	chr1:227612340-227612390	HAEpiC	amniotic membrane:	n/a
4	chr1:227612340-227612390	ovcar-3	ovarian:	n/a
5	chr1:227612340-227612390	PrEC	prostate:	n/a
6	chr1:227612340-227612390	ProgFib	skin:	n/a
7	chr1:227612340-227612390	NH-A	brain:	n/a
8	chr1:227612340-227612390	AG04449	skin:	fetal
9	chr1:227612340-227612390	BE2_C	brain:	n/a
10	chr1:227612340-227612390	SKMC	muscle:	n/a
11	chr1:227612340-227612390	HPAEpiC	pulmonary alveolar:	n/a
12	chr1:227612340-227612390	BJ	skin:	n/a
13	chr1:227612340-227612390	GM12891	blood:	n/a
14	chr1:227612340-227612390	HEEpiC	esophagus:	n/a
15	chr1:227612340-227612390	AG04450	lung:	fetal
16	chr1:227612340-227612390	HUVEC	blood vessel:	n/a
17	chr1:227612340-227612390	PFSK-1	brain:	n/a
18	chr1:227612340-227612390	SK-N-SH	brain:	n/a
19	chr1:227612340-227612390	AG09309	skin:	n/a
20	chr1:227612340-227612390	HRPEpiC	eye:	n/a
21	chr1:227612340-227612390	GM12892	blood:	n/a
22	chr1:227612340-227612390	SK-N-SH_RA	brain:	n/a
23	chr1:227612340-227612390	GM12878	blood:	n/a
24	chr1:227612340-227612390	Jurkat	blood:	n/a
25	chr1:227612340-227612390	HEK293	kidney:	embryo
26	chr1:227612340-227612390	U87	brain:	n/a
27	chr1:227612340-227612390	NT2-D1	testis:	n/a
28	chr1:227612340-227612390	SAEC	small airway:	n/a
29	chr1:227612340-227612390	HRE	kidney:	n/a
30	chr1:227612340-227612390	Hela-S3	cervix:	n/a
31	chr1:227612340-227612390	AoSMC	blood vessel:	n/a
32	chr1:227612340-227612390	NHDF-neo	bronchial:	n/a
33	chr1:227612340-227612390	LNCaP	prostate:	n/a
34	chr1:227612340-227612390	K562	blood:	n/a
35	chr1:227612340-227612390	PANC-1	pancreas:	n/a
36	chr1:227612340-227612390	HCPEpiC	choroid plexus:	n/a
37	chr1:227612340-227612390	AG09319	gingival:	n/a
38	chr1:227612340-227612390	HCT-116	colon:	n/a
39	chr1:227612340-227612390	HMEC	breast:	n/a
40	chr1:227612340-227612390	ECC-1	luminal epithelium:	n/a
41	chr1:227612340-227612390	Hepatocyte	liver:	n/a
42	chr1:227612340-227612390	MCF-7	breast:	n/a
43	chr1:227612340-227612390	Caco-2	colon:	n/a
44	chr1:227612340-227612390	HNPCEpiC	eye:	n/a
45	chr1:227612340-227612390	HIPEpiC	eye:	n/a
46	chr1:227612340-227612390	NHBE	bronchial:	n/a
47	chr1:227612340-227612390	RPTEC	kidney:	n/a
48	chr1:227612340-227612390	IMR90	lung:	fetal
49	chr1:227612340-227612390	HepG2	liver:	n/a
50	chr1:227612340-227612390	GM06990	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:227505439..227506978-chr1:227600275..227602488,2	MCF-7	breast:
2	chr1:227578119..227581046-chr11:66042464..66044320,2	MCF-7	breast:
3	chr1:227614393..227617213-chr1:227617551..227619709,2	K562	blood:
4	chr1:227604475..227606145-chr1:227609064..227610795,2	MCF-7	breast:
5	chr1:227506036..227507932-chr1:227615818..227619997,3	MCF-7	breast:
6	chr1:227506033..227508840-chr1:227610999..227613021,2	MCF-7	breast:
7	chr1:227601371..227603853-chr1:227605380..227608209,2	K562	blood:
8	chr1:227545250..227546932-chr1:227614922..227616911,2	K562	blood:
9	chr1:227596112..227598714-chr1:227598810..227600667,2	K562	blood:
10	chr1:227604475..227606145-chr1:227609064..227610795,2	MCF-7	breast:
11	chr1:227606920..227609414-chr1:227610564..227613546,2	MCF-7	breast:
12	chr1:227605581..227608892-chr1:227610370..227614141,3	K562	blood:
13	chr1:227504042..227507688-chr1:227616722..227620233,4	K562	blood:
14	chr1:227583675..227585639-chr1:227602382..227605024,2	K562	blood:
15	chr1:227615713..227617312-chr1:227617551..227620408,2	K562	blood:
16	chr1:227606920..227609414-chr1:227610564..227613546,2	MCF-7	breast:
17	chr1:227611022..227613479-chr1:227613534..227615675,2	K562	blood:
18	chr1:227567329..227569359-chr1:227583309..227586812,3	K562	blood:
19	chr1:227583443..227586949-chr1:227620291..227624641,4	K562	blood:
20	chr1:227504778..227506670-chr1:227579538..227582289,3	K562	blood:
21	chr1:227502664..227506000-chr1:227614343..227617571,3	K562	blood:
22	chr1:227583675..227585639-chr1:227602382..227605024,2	K562	blood:
23	chr1:227588107..227590811-chr1:227609201..227611175,2	MCF-7	breast:
24	chr1:227597318..227599124-chr1:227602083..227603955,3	K562	blood:
25	chr1:227573402..227580584-chr1:227581981..227587587,10	K562	blood:
26	chr1:227421745..227423708-chr1:227616261..227618228,2	MCF-7	breast:
27	chr1:227598952..227600473-chr1:227602065..227604996,2	K562	blood:
28	chr1:227581289..227584250-chr1:227584710..227586492,2	MCF-7	breast:
29	chr1:227588107..227590811-chr1:227609201..227611175,2	MCF-7	breast:
30	chr1:227504778..227506536-chr1:227579859..227582289,2	K562	blood:
31	chr1:227601371..227603853-chr1:227605380..227608209,2	K562	blood:
32	chr1:227612197..227614219-chr1:227619414..227621480,2	MCF-7	breast:
33	chr1:227505922..227508006-chr1:227610369..227612808,3	K562	blood:
34	chr1:227596112..227598714-chr1:227598810..227600667,2	K562	blood:
35	chr1:227611022..227613479-chr1:227613534..227615675,2	K562	blood:
36	chr1:227607546..227609954-chr1:227617674..227619655,2	K562	blood:
37	chr1:227506125..227508936-chr1:227583007..227585460,2	K562	blood:
38	chr1:227605581..227608892-chr1:227610370..227614141,3	K562	blood:
39	chr1:227505544..227508414-chr1:227579779..227582450,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF678-1	chr1:227597456-227597585	NONHSAT009921
2	lnc-ZNF678-1	chr1:227617106-227618736	ENSG00000234277.2
3	lnc-ZNF678-1	chr1:227581308-227581405	NONHSAT009921
4	lnc-ZNF678-1	chr1:227613457-227613758	ENSG00000234277.2
5	lnc-ZNF678-4	chr1:227610210-227610238	l_205_chr1:227610209-227612763_76bGuttman_hES
6	lnc-ZNF678-1	chr1:227581292-227581405	ENSG00000234277.2
7	lnc-ZNF678-1	chr1:227583220-227583315	ENSG00000234277.2
8	lnc-ZNF678-4	chr1:227612472-227612763	l_205_chr1:227610209-227612763_76bGuttman_hES
9	lnc-ZNF678-1	chr1:227597456-227597585	ENSG00000234277.2
10	lnc-ZNF678-1	chr1:227605037-227605371	NONHSAT009921
11	lnc-ZNF678-1	chr1:227597466-227597585	ENSG00000234277.2

No data

Variant related genes	Relation type
ENSG00000234277	TF binding region
ENSG00000232864	TF binding region
ENSG00000242757	TF binding region
BTF3P9	TF binding region
ENSG00000234277	CpG island
ENSG00000232864	CpG island
ENSG00000242757	CpG island
BTF3P9	CpG island
ENSG00000232864	chromatin interactions
ENSG00000242757	chromatin interactions
ENSG00000224834	chromatin interactions
ENSG00000234277	chromatin interactions
ENSG00000143776	chromatin interactions
ENSG00000228729	chromatin interactions

Extended variants
information (count: 1160 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4606283	chr1:227581017-227581018	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
2	rs539363335	chr1:227581071-227581072	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs76303943	chr1:227581093-227581094	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs370727243	chr1:227581102-227581103	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs558882516	chr1:227581118-227581119	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs4491034	chr1:227581211-227581212	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs189831193	chr1:227581212-227581213	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs149870973	chr1:227581227-227581228	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs143860934	chr1:227581297-227581298	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs10916137	chr1:227581308-227581309	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs571521977	chr1:227581321-227581322	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs140646397	chr1:227581428-227581429	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543364639	chr1:227581446-227581447	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs181211786	chr1:227581460-227581461	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185656732	chr1:227581484-227581485	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs557333380	chr1:227581491-227581492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577053795	chr1:227581505-227581506	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554457677	chr1:227581515-227581516	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs11811982	chr1:227581520-227581521	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs536703252	chr1:227581558-227581559	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs558643672	chr1:227581566-227581567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576398059	chr1:227581574-227581575	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs4233227	chr1:227581580-227581581	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs552595151	chr1:227581635-227581636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs572393165	chr1:227581664-227581665	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs543312039	chr1:227581665-227581666	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs561275671	chr1:227581697-227581698	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs190064843	chr1:227581731-227581732	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs58687385	chr1:227581760-227581761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs111968937	chr1:227581807-227581808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs542060413	chr1:227581848-227581849	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs565362726	chr1:227581858-227581859	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs182309031	chr1:227581862-227581863	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200547509	chr1:227581872-227581873	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs4653833	chr1:227581912-227581913	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs376125951	chr1:227581951-227581952	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs566121876	chr1:227582056-227582057	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs147824678	chr1:227582170-227582171	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs202191416	chr1:227582187-227582188	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs112412638	chr1:227582188-227582189	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs67679713	chr1:227582189-227582190	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs58712091	chr1:227582190-227582191	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs185859799	chr1:227582200-227582201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569725715	chr1:227582201-227582202	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537270302	chr1:227582202-227582203	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs10399722	chr1:227582203-227582204	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs192379185	chr1:227582228-227582229	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs141289631	chr1:227582238-227582239	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs111510444	chr1:227582247-227582248	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs183691462	chr1:227582265-227582266	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227576800-227584600	Weak transcription	A549	lung
2	chr1:227577000-227583200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:227577800-227583200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr1:227578400-227583200	Weak transcription	HSMMtube	muscle
5	chr1:227579800-227583600	Weak transcription	Stomach Mucosa	stomach
6	chr1:227580200-227585000	Weak transcription	HUVEC	blood vessel
7	chr1:227581000-227581200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:227581000-227581800	Enhancers	K562	blood
9	chr1:227581800-227582800	Weak transcription	K562	blood
10	chr1:227582800-227583600	Enhancers	K562	blood
11	chr1:227583200-227583600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:227583200-227583800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:227583200-227583800	Enhancers	HSMMtube	muscle
14	chr1:227583600-227584800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:227583600-227585400	Enhancers	Stomach Mucosa	stomach
16	chr1:227583600-227585400	Flanking Active TSS	K562	blood
17	chr1:227583800-227584400	Enhancers	HMEC	breast
18	chr1:227583800-227584600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr1:227584200-227585200	Enhancers	Thymus	Thymus
20	chr1:227584200-227585400	Enhancers	Primary T cells from cord blood	blood
21	chr1:227584400-227584800	Enhancers	HepG2	liver
22	chr1:227584600-227585400	Enhancers	A549	lung
23	chr1:227584800-227585000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:227585000-227587600	Enhancers	HUVEC	blood vessel
25	chr1:227585400-227587600	Enhancers	K562	blood
26	chr1:227585400-227589000	Weak transcription	Stomach Mucosa	stomach
27	chr1:227589000-227590000	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr1:227589000-227590000	Enhancers	Stomach Mucosa	stomach
29	chr1:227598200-227599200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:227599200-227603200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:227602600-227604000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:227602800-227603400	Enhancers	Primary hematopoietic stem cells	blood
33	chr1:227602800-227603800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr1:227602800-227604000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:227602800-227604600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:227603000-227603200	Enhancers	Left Ventricle	heart
37	chr1:227603000-227604200	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr1:227603000-227604600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:227603200-227604400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:227603400-227604000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:227603600-227604200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr1:227603600-227604400	Enhancers	Osteobl	bone
43	chr1:227604200-227605400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:227604200-227605600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr1:227604200-227606000	Weak transcription	Left Ventricle	heart
46	chr1:227604600-227605600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr1:227605000-227606200	Enhancers	Fetal Intestine Large	intestine
48	chr1:227605200-227606000	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr1:227605200-227606200	Enhancers	Adipose Nuclei	Adipose
50	chr1:227605200-227606200	Enhancers	Fetal Intestine Small	intestine

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