Variant report

Variant	esv1806604
Chromosome Location	chr1:212468974-212505860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:343)
CpG islands
(count:122)
Chromatin interactive
region (count:25)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:343 , 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	chr1:212483372-212483625	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:212489252-212489485	K562	blood:	n/a	n/a
3	ATF1	chr1:212497635-212497677	K562	blood:	n/a	n/a
4	ATF1	chr1:212489306-212489436	K562	blood:	n/a	n/a
5	ATF1	chr1:212469803-212470088	K562	blood:	n/a	n/a
6	BATF	chr1:212489356-212489694	GM12878	blood:	n/a	n/a
7	BATF	chr1:212476325-212476640	GM12878	blood:	n/a	n/a
8	CEBPB	chr1:212501658-212501829	A549	lung:	n/a	chr1:212501765-212501776
9	CEBPB	chr1:212482109-212482110	K562	blood:	n/a	n/a
10	CEBPB	chr1:212485527-212485723	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:212483402-212483560	Hela-S3	cervix:	n/a	chr1:212483488-212483499
12	CEBPB	chr1:212483314-212483682	H1-hESC	embryonic stem cell:	n/a	chr1:212483488-212483499
13	CEBPB	chr1:212501692-212501880	K562	blood:	n/a	chr1:212501765-212501776
14	CEBPB	chr1:212501619-212501892	IMR90	lung:	n/a	chr1:212501765-212501776
15	CEBPB	chr1:212485452-212485763	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:212501669-212501869	HepG2	liver:	n/a	chr1:212501765-212501776
17	CEBPB	chr1:212483395-212483558	HepG2	liver:	n/a	chr1:212483488-212483499
18	CEBPB	chr1:212483315-212483665	HepG2	liver:	n/a	chr1:212483488-212483499
19	CEBPD	chr1:212483377-212483612	HepG2	liver:	n/a	n/a
20	CHD1	chr1:212479005-212479009	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr1:212484295-212484306	GM12878	blood:	n/a	n/a
22	CTCF	chr1:212489320-212489470	HPF	lung:	n/a	n/a
23	CTCF	chr1:212489120-212489270	HAc	cerebellar:	n/a	n/a
24	CTCF	chr1:212489280-212489430	SAEC	small airway:	n/a	n/a
25	CTCF	chr1:212489273-212489459	NHEK	skin:	n/a	n/a
26	CTCF	chr1:212489235-212489503	MCF-7	breast:	n/a	n/a
27	CTCF	chr1:212489300-212489450	HCT-116	colon:	n/a	n/a
28	CTCF	chr1:212489257-212489463	HepG2	liver:	n/a	n/a
29	CTCF	chr1:212482640-212482790	HEK293	kidney:	n/a	n/a
30	CTCF	chr1:212489340-212489490	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr1:212489280-212489430	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr1:212489240-212489390	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr1:212489254-212489472	K562	blood:	n/a	n/a
34	CTCF	chr1:212489316-212489447	GM13977	blood:	n/a	n/a
35	CTCF	chr1:212489340-212489490	BE2_C	brain:	n/a	n/a
36	CTCF	chr1:212489240-212489390	GM12872	blood:	n/a	n/a
37	CTCF	chr1:212489247-212489462	GM12878	blood:	n/a	n/a
38	CTCF	chr1:212489340-212489490	GM12872	blood:	n/a	n/a
39	CTCF	chr1:212489220-212489370	GM12874	blood:	n/a	n/a
40	CTCF	chr1:212489211-212489522	K562	blood:	n/a	n/a
41	CTCF	chr1:212489320-212489470	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr1:212489280-212489430	AG10803	skin:	n/a	n/a
43	CTCF	chr1:212504560-212504710	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr1:212489260-212489410	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr1:212489300-212489450	GM12874	blood:	n/a	n/a
46	CTCF	chr1:212489220-212489370	GM12865	blood:	n/a	n/a
47	CTCF	chr1:212489281-212489454	A549	lung:	n/a	n/a
48	CTCF	chr1:212489220-212489370	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr1:212489260-212489410	A549	lung:	n/a	n/a
50	CTCF	chr1:212489172-212489540	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:212483036-212483086	SKMC	muscle:	n/a
2	chr1:212483036-212483086	HUVEC	blood vessel:	n/a
3	chr1:212482804-212482854	NT2-D1	testis:	n/a
4	chr1:212482804-212482854	MCF10A-Er-Src	breast:	n/a
5	chr1:212483036-212483086	U87	brain:	n/a
6	chr1:212483036-212483086	HIPEpiC	eye:	n/a
7	chr1:212483036-212483086	MCF10A-Er-Src	breast:	n/a
8	chr1:212483036-212483086	HRPEpiC	eye:	n/a
9	chr1:212482804-212482854	HL-60	blood:	n/a
10	chr1:212483036-212483086	Caco-2	colon:	n/a
11	chr1:212483036-212483086	HAEpiC	amniotic membrane:	n/a
12	chr1:212482804-212482854	AG10803	skin:	n/a
13	chr1:212482804-212482854	Jurkat	blood:	n/a
14	chr1:212483036-212483086	H1-hESC	embryonic stem cell:	embryo
15	chr1:212482804-212482854	HIPEpiC	eye:	n/a
16	chr1:212482804-212482854	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:212483036-212483086	GM12892	blood:	n/a
18	chr1:212483036-212483086	BJ	skin:	n/a
19	chr1:212483036-212483086	HNPCEpiC	eye:	n/a
20	chr1:212482804-212482854	ECC-1	luminal epithelium:	n/a
21	chr1:212483036-212483086	NT2-D1	testis:	n/a
22	chr1:212483036-212483086	T-47D	breast:	n/a
23	chr1:212483036-212483086	CMK	blood:	n/a
24	chr1:212483036-212483086	Hepatocyte	liver:	n/a
25	chr1:212483036-212483086	SAEC	small airway:	n/a
26	chr1:212482804-212482854	HEEpiC	esophagus:	n/a
27	chr1:212483036-212483086	LNCaP	prostate:	n/a
28	chr1:212482804-212482854	AG04450	lung:	fetal
29	chr1:212483036-212483086	NHDF-neo	bronchial:	n/a
30	chr1:212483036-212483086	HRE	kidney:	n/a
31	chr1:212482804-212482854	AG04449	skin:	fetal
32	chr1:212482804-212482854	BJ	skin:	n/a
33	chr1:212482804-212482854	ovcar-3	ovarian:	n/a
34	chr1:212482804-212482854	PrEC	prostate:	n/a
35	chr1:212483036-212483086	HCM	heart:	n/a
36	chr1:212482804-212482854	HRPEpiC	eye:	n/a
37	chr1:212482804-212482854	NB4	blood:	n/a
38	chr1:212483036-212483086	HCPEpiC	choroid plexus:	n/a
39	chr1:212483036-212483086	NHBE	bronchial:	n/a
40	chr1:212482804-212482854	NHBE	bronchial:	n/a
41	chr1:212482804-212482854	T-47D	breast:	n/a
42	chr1:212483036-212483086	GM06990	blood:	n/a
43	chr1:212482804-212482854	GM12878	blood:	n/a
44	chr1:212482804-212482854	RPTEC	kidney:	n/a
45	chr1:212483036-212483086	AG04450	lung:	fetal
46	chr1:212482804-212482854	SK-N-SH_RA	brain:	n/a
47	chr1:212483036-212483086	HEK293	kidney:	embryo
48	chr1:212483036-212483086	AG10803	skin:	n/a
49	chr1:212482804-212482854	GM19239	blood:	n/a
50	chr1:212483036-212483086	HRCEpiC	kidney:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:212487148..212489947-chr1:212490208..212492615,2	K562	blood:
2	chr1:212458179..212461162-chr1:212476171..212477846,2	K562	blood:
3	chr1:212498492..212500161-chr1:212502624..212504946,2	K562	blood:
4	chr1:212497077..212499015-chr1:212500342..212502392,2	K562	blood:
5	chr1:212497277..212499052-chr1:212502846..212504617,2	K562	blood:
6	chr1:212487148..212489947-chr1:212490208..212492615,2	K562	blood:
7	chr1:212458786..212460373-chr1:212467150..212468979,2	MCF-7	breast:
8	chr1:212480848..212483248-chr1:212485373..212487315,2	K562	blood:
9	chr1:212458610..212460865-chr1:212476520..212479073,2	K562	blood:
10	chr1:212486882..212489433-chr1:212500849..212503303,2	K562	blood:
11	chr1:212457668..212459740-chr1:212480446..212483252,3	MCF-7	breast:
12	chr1:212207874..212210516-chr1:212490842..212492597,2	K562	blood:
13	chr1:212207316..212210086-chr1:212486077..212488983,2	MCF-7	breast:
14	chr1:212467247..212471909-chr1:212472711..212476183,6	K562	blood:
15	chr1:212456717..212458394-chr1:212483325..212485097,2	MCF-7	breast:
16	chr1:212464978..212469431-chr1:212471345..212474474,8	K562	blood:
17	chr1:212464978..212469431-chr1:212471345..212474474,8	K562	blood:
18	chr1:212498492..212500161-chr1:212502624..212504946,2	K562	blood:
19	chr1:212458567..212461041-chr1:212484616..212487117,2	MCF-7	breast:
20	chr1:212467247..212471909-chr1:212472711..212476183,6	K562	blood:
21	chr1:212497077..212499015-chr1:212500342..212502392,2	K562	blood:
22	chr1:212505148..212507116-chr1:212513885..212516139,2	MCF-7	breast:
23	chr1:212486882..212489433-chr1:212500849..212503303,2	K562	blood:
24	chr1:212497277..212499052-chr1:212502846..212504617,2	K562	blood:
25	chr1:212208039..212208902-chr1:212488872..212489422,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NENF-4	chr1:212492719-212492887	NONHSAT009362
2	lnc-NENF-4	chr1:212475205-212475434	NONHSAT009362
3	lnc-TMEM206-3	chr1:212504800-212505055	ENSG00000234915.1
4	lnc-TMEM206-3	chr1:212504902-212504941	l_184_chr1:212497765-212519010_heart
5	lnc-NENF-4	chr1:212492719-212492894	NONHSAT009363
6	lnc-NENF-4	chr1:212485015-212485041	NONHSAT009363
7	lnc-TMEM206-3	chr1:212497766-212502930	l_184_chr1:212497765-212519010_heart
8	lnc-TMEM206-3	chr1:212472837-212472967	ENSG00000234915.1
9	lnc-NENF-2	chr1:212470790-212471143	ENSG00000230063.1
10	lnc-NENF-2	chr1:212472626-212472921	ENSG00000230063.1

No data

Variant related genes	Relation type
ENSG00000225338	TF binding region
ENSG00000230063	TF binding region
ENSG00000234915	TF binding region
PPP2R5A	TF binding region
ENSG00000225338	CpG island
ENSG00000230063	CpG island
ENSG00000234915	CpG island
PPP2R5A	CpG island
ENSG00000225338	chromatin interactions
ENSG00000230063	chromatin interactions
ENSG00000143476	chromatin interactions
ENSG00000143493	chromatin interactions
ENSG00000066027	chromatin interactions

Extended variants
information (count: 1252 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1252 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs411278	chr1:212468974-212468975	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552785952	chr1:212468992-212468993	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs570962183	chr1:212469003-212469004	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs437701	chr1:212469010-212469011	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
5	rs74138127	chr1:212469111-212469112	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs414197	chr1:212469120-212469121	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs35519200	chr1:212469136-212469137	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs535111898	chr1:212469216-212469217	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs553640986	chr1:212469280-212469281	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs565684428	chr1:212469336-212469337	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs539354035	chr1:212469343-212469344	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs148623825	chr1:212469355-212469356	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552303388	chr1:212469357-212469358	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs550162866	chr1:212469401-212469402	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs576175271	chr1:212469420-212469421	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs79388349	chr1:212469454-212469455	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
17	rs144204658	chr1:212469465-212469466	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs528442196	chr1:212469504-212469505	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs147760790	chr1:212469525-212469526	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560766427	chr1:212469565-212469566	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548434248	chr1:212469572-212469573	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527944354	chr1:212469595-212469596	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs546191404	chr1:212469602-212469603	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs377183746	chr1:212469645-212469646	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs368919618	chr1:212469646-212469647	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs139573880	chr1:212469691-212469692	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs549830159	chr1:212469720-212469721	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs561484150	chr1:212469866-212469867	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs528854419	chr1:212469889-212469890	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546941602	chr1:212469896-212469897	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs112589676	chr1:212470004-212470005	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs17042040	chr1:212470027-212470028	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs574735891	chr1:212470109-212470110	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs542323590	chr1:212470192-212470193	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373362426	chr1:212470233-212470234	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551410633	chr1:212470234-212470235	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569812336	chr1:212470256-212470257	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs111498415	chr1:212470257-212470258	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568095203	chr1:212470301-212470302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12124582	chr1:212470340-212470341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs2358448	chr1:212470400-212470401	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs182186386	chr1:212470412-212470413	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs12069850	chr1:212470436-212470437	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs531756312	chr1:212470453-212470454	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs410461	chr1:212470455-212470456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs371299978	chr1:212470456-212470457	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs149712251	chr1:212470459-212470460	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs143835959	chr1:212470462-212470463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs71137738	chr1:212470466-212470467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs386417852	chr1:212470481-212470482	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
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
Acute lymphoblastic leukemia	17443227	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
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
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:958 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212460200-212489200	Weak transcription	Spleen	Spleen
2	chr1:212461000-212469000	Enhancers	Brain Substantia Nigra	brain
3	chr1:212461000-212476200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:212461800-212470200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr1:212462000-212471200	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr1:212462200-212471000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr1:212462200-212471000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr1:212462400-212469000	Enhancers	Brain Cingulate Gyrus	brain
9	chr1:212462600-212471000	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr1:212462800-212470000	Enhancers	Liver	Liver
11	chr1:212463800-212471000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr1:212463800-212471000	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr1:212464200-212471200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr1:212464200-212483000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr1:212464600-212473000	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr1:212464800-212480200	Weak transcription	Lung	lung
17	chr1:212464800-212483800	Weak transcription	Pancreas	Pancrea
18	chr1:212464800-212506400	Weak transcription	Esophagus	oesophagus
19	chr1:212465000-212469600	Enhancers	Adipose Nuclei	Adipose
20	chr1:212465000-212470400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr1:212465000-212474800	Weak transcription	Osteobl	bone
22	chr1:212465000-212480200	Weak transcription	Primary hematopoietic stem cells	blood
23	chr1:212465400-212475000	Weak transcription	Rectal Smooth Muscle	rectum
24	chr1:212465400-212482800	Weak transcription	Fetal Lung	lung
25	chr1:212465800-212483200	Weak transcription	Dnd41	blood
26	chr1:212466200-212470400	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr1:212466200-212470600	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr1:212466200-212473000	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr1:212466200-212506400	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr1:212466400-212470200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr1:212466600-212479400	Weak transcription	NHEK	skin
32	chr1:212466600-212482600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr1:212466600-212503000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr1:212466800-212469000	Enhancers	Fetal Heart	heart
35	chr1:212466800-212470000	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr1:212467000-212472800	Weak transcription	Primary B cells from cord blood	blood
37	chr1:212467000-212473400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:212467000-212480800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr1:212467200-212469000	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr1:212467200-212470400	Enhancers	GM12878-XiMat	blood
41	chr1:212467200-212470600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:212467200-212474800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr1:212467200-212475000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr1:212467200-212481800	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr1:212467400-212469000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr1:212467400-212474800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr1:212467400-212480200	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr1:212467400-212482800	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr1:212467400-212526000	Weak transcription	A549	lung
50	chr1:212467600-212482800	Weak transcription	HepG2	liver

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