Variant report

Variant	esv3326671
Chromosome Location	chr2:37383073-37385621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:385)
CpG islands
(count:859)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37384085-37384486	HepG2	liver:	n/a	n/a
2	ATF2	chr2:37384017-37384384	GM12878	blood:	n/a	n/a
3	BHLHE40	chr2:37383642-37383842	K562	blood:	n/a	n/a
4	BHLHE40	chr2:37384086-37384414	GM12878	blood:	n/a	chr2:37384149-37384165
5	BHLHE40	chr2:37384111-37384500	HepG2	liver:	n/a	chr2:37384149-37384165
6	BRCA1	chr2:37383263-37384388	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr2:37384045-37384415	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr2:37384010-37384349	GM12878	blood:	n/a	n/a
9	BRCA1	chr2:37384014-37384348	HepG2	liver:	n/a	n/a
10	BRCA1	chr2:37383351-37383369	GM12878	blood:	n/a	n/a
11	CBX3	chr2:37384013-37384338	K562	blood:	n/a	n/a
12	CCNT2	chr2:37383181-37384423	K562	blood:	n/a	chr2:37384340-37384349 chr2:37384001-37384010
13	CEBPB	chr2:37383198-37383804	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr2:37384509-37384741	K562	blood:	n/a	n/a
15	CEBPB	chr2:37384593-37384605	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr2:37384495-37384875	HepG2	liver:	n/a	n/a
17	CEBPD	chr2:37383851-37384570	HepG2	liver:	n/a	n/a
18	CHD1	chr2:37383725-37383938	GM12878	blood:	n/a	n/a
19	CHD1	chr2:37383716-37384226	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr2:37384297-37384534	GM12878	blood:	n/a	n/a
21	CHD2	chr2:37383988-37384482	K562	blood:	n/a	n/a
22	CHD2	chr2:37383726-37384391	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr2:37384003-37384535	GM12878	blood:	n/a	n/a
24	CHD2	chr2:37383811-37384653	HepG2	liver:	n/a	n/a
25	CHD2	chr2:37383519-37384673	Hela-S3	cervix:	n/a	n/a
26	CREB1	chr2:37383897-37384403	A549	lung:	n/a	n/a
27	CTCF	chr2:37383780-37383930	HepG2	liver:	n/a	chr2:37383897-37383910
28	CTCF	chr2:37384468-37384579	K562	blood:	n/a	n/a
29	CTCF	chr2:37384076-37384091	GM10266	blood:	n/a	n/a
30	CTCF	chr2:37384040-37384190	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr2:37383840-37383990	WERI-Rb-1	eye:	n/a	chr2:37383897-37383910
32	CTCF	chr2:37384126-37384209	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr2:37384520-37384670	HepG2	liver:	n/a	n/a
34	CTCF	chr2:37384100-37384250	AG04449	skin:	n/a	n/a
35	CTCF	chr2:37384460-37384610	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr2:37383140-37383290	GM12875	blood:	n/a	n/a
37	CTCF	chr2:37383760-37383910	AG04449	skin:	n/a	chr2:37383897-37383910
38	CTCF	chr2:37384120-37384270	NHEK	skin:	n/a	n/a
39	CTCF	chr2:37384131-37384231	GM12878	blood:	n/a	n/a
40	CTCF	chr2:37384640-37384790	HepG2	liver:	n/a	n/a
41	CTCF	chr2:37383980-37384130	GM06990	blood:	n/a	n/a
42	E2F1	chr2:37384015-37384456	Hela-S3	cervix:	n/a	chr2:37384340-37384349 chr2:37384224-37384235 chr2:37384151-37384161
43	E2F4	chr2:37384058-37384636	MCF10A-Er-Src	breast:	n/a	chr2:37384340-37384349 chr2:37384151-37384161
44	E2F6	chr2:37384021-37384701	A549	lung:	n/a	chr2:37384340-37384349 chr2:37384151-37384161
45	E2F6	chr2:37383971-37384416	A549	lung:	n/a	chr2:37384340-37384349 chr2:37384151-37384161
46	E2F6	chr2:37384056-37384394	K562	blood:	n/a	chr2:37384340-37384349 chr2:37384151-37384161
47	E2F6	chr2:37384025-37384663	K562	blood:	n/a	chr2:37384340-37384349 chr2:37384151-37384161
48	E2F6	chr2:37383975-37384522	H1-hESC	embryonic stem cell:	n/a	chr2:37384340-37384349 chr2:37384151-37384161
49	E2F6	chr2:37383920-37384635	H1-hESC	embryonic stem cell:	n/a	chr2:37384340-37384349 chr2:37384151-37384161
50	EBF1	chr2:37384074-37384487	GM12878	blood:	n/a	n/a

(count:859 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37384227-37384277	AG10803	skin:	n/a
2	chr2:37384523-37384573	GM06990	blood:	n/a
3	chr2:37384171-37384221	HUVEC	blood vessel:	n/a
4	chr2:37384401-37384451	SK-N-SH	brain:	n/a
5	chr2:37384231-37384281	GM06990	blood:	n/a
6	chr2:37384227-37384277	AG10803	skin:	n/a
7	chr2:37384523-37384573	GM06990	blood:	n/a
8	chr2:37384171-37384221	HUVEC	blood vessel:	n/a
9	chr2:37384401-37384451	SK-N-SH	brain:	n/a
10	chr2:37384231-37384281	GM06990	blood:	n/a
11	chr2:37384227-37384277	T-47D	breast:	n/a
12	chr2:37384523-37384573	GM12892	blood:	n/a
13	chr2:37384244-37384294	SAEC	small airway:	n/a
14	chr2:37384227-37384277	NB4	blood:	n/a
15	chr2:37384227-37384277	NHDF-neo	bronchial:	n/a
16	chr2:37384401-37384451	HL-60	blood:	n/a
17	chr2:37384171-37384221	HCF	heart:	n/a
18	chr2:37383994-37384044	HCF	heart:	n/a
19	chr2:37383994-37384044	Hepatocyte	liver:	n/a
20	chr2:37384401-37384451	SK-N-SH_RA	brain:	n/a
21	chr2:37383994-37384044	MCF-7	breast:	n/a
22	chr2:37384244-37384294	NH-A	brain:	n/a
23	chr2:37384231-37384281	ovcar-3	ovarian:	n/a
24	chr2:37384248-37384298	AG09309	skin:	n/a
25	chr2:37384229-37384279	HEK293	kidney:	embryo
26	chr2:37383994-37384044	GM06990	blood:	n/a
27	chr2:37384229-37384279	AG09309	skin:	n/a
28	chr2:37384286-37384336	PANC-1	pancreas:	n/a
29	chr2:37384227-37384277	SK-N-SH_RA	brain:	n/a
30	chr2:37384244-37384294	HEEpiC	esophagus:	n/a
31	chr2:37384248-37384298	NB4	blood:	n/a
32	chr2:37384381-37384431	SKMC	muscle:	n/a
33	chr2:37384286-37384336	HCT-116	colon:	n/a
34	chr2:37384171-37384221	CMK	blood:	n/a
35	chr2:37384401-37384451	BE2_C	brain:	n/a
36	chr2:37384381-37384431	HRPEpiC	eye:	n/a
37	chr2:37384227-37384277	ovcar-3	ovarian:	n/a
38	chr2:37384229-37384279	PrEC	prostate:	n/a
39	chr2:37384244-37384294	HCM	heart:	n/a
40	chr2:37384248-37384298	ProgFib	skin:	n/a
41	chr2:37384231-37384281	AG10803	skin:	n/a
42	chr2:37384381-37384431	HEEpiC	esophagus:	n/a
43	chr2:37384227-37384277	AG04449	skin:	fetal
44	chr2:37384244-37384294	GM12892	blood:	n/a
45	chr2:37384248-37384298	SAEC	small airway:	n/a
46	chr2:37384244-37384294	HRPEpiC	eye:	n/a
47	chr2:37384248-37384298	RPTEC	kidney:	n/a
48	chr2:37384171-37384221	SAEC	small airway:	n/a
49	chr2:37384401-37384451	RPTEC	kidney:	n/a
50	chr2:37384286-37384336	NB4	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:37381640..37387428-chr2:37421417..37425727,6	MCF-7	breast:
2	chr2:37385569..37388130-chr2:37422191..37423882,2	K562	blood:
3	chr2:37353750..37355399-chr2:37381994..37383534,2	MCF-7	breast:
4	chr2:37382080..37383766-chr2:37457653..37460217,2	MCF-7	breast:
5	chr2:37370415..37372075-chr2:37384482..37387450,2	K562	blood:
6	chr2:37372644..37374273-chr2:37382533..37385006,2	K562	blood:
7	chr2:37375493..37378915-chr2:37383921..37387868,3	K562	blood:
8	chr2:37382658..37387385-chr2:37421093..37425812,6	MCF-7	breast:
9	chr2:37373517..37380041-chr2:37380520..37385811,10	MCF-7	breast:
10	chr2:37374955..37377720-chr2:37382756..37385654,3	MCF-7	breast:
11	chr2:37383967..37386325-chr2:37457482..37459560,2	MCF-7	breast:
12	chr2:37385156..37387851-chr2:37415682..37418467,2	K562	blood:

No data

Variant related genes	Relation type
EIF2AK2	TF binding region
EIF2AK2	CpG island
ENSG00000003509	chromatin interactions
ENSG00000224891	chromatin interactions
ENSG00000138068	chromatin interactions
ENSG00000115816	chromatin interactions
ENSG00000233159	chromatin interactions
ENSG00000218739	chromatin interactions
ENSG00000055332	chromatin interactions

Extended variants
information (count: 92 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540431033	chr2:37383076-37383077	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs74698719	chr2:37383093-37383094	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs70949736	chr2:37383097-37383098	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs201980021	chr2:37383098-37383099	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs532662016	chr2:37383138-37383139	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs550888143	chr2:37383153-37383154	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs4670666	chr2:37383166-37383167	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs530009859	chr2:37383239-37383240	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs12712526	chr2:37383315-37383316	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs78914684	chr2:37383390-37383391	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs192326827	chr2:37383448-37383449	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs546807423	chr2:37383479-37383480	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs571514611	chr2:37383522-37383523	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs184662377	chr2:37383542-37383543	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs13008681	chr2:37383625-37383626	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs115509351	chr2:37383682-37383683	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs535824504	chr2:37383706-37383707	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs149073456	chr2:37383727-37383728	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs142876454	chr2:37383771-37383772	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs11899117	chr2:37383772-37383773	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs565113590	chr2:37383790-37383791	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs11904602	chr2:37383830-37383831	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs544415496	chr2:37383868-37383869	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs572686720	chr2:37383898-37383899	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs562816675	chr2:37383900-37383901	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs530428103	chr2:37384001-37384002	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs539954844	chr2:37384007-37384008	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs541820062	chr2:37384040-37384041	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs564207041	chr2:37384053-37384054	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs376636931	chr2:37384054-37384055	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs560574348	chr2:37384061-37384062	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs57835937	chr2:37384085-37384086	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs112719085	chr2:37384108-37384109	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs552733788	chr2:37384117-37384118	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs571453196	chr2:37384179-37384180	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs532317149	chr2:37384193-37384194	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs550796996	chr2:37384194-37384195	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs569013845	chr2:37384199-37384200	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs536586330	chr2:37384213-37384214	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs111463611	chr2:37384240-37384241	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs189126736	chr2:37384245-37384246	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs573303340	chr2:37384248-37384249	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs544154430	chr2:37384254-37384255	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs12992188	chr2:37384283-37384284	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs62133148	chr2:37384296-37384297	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs13018861	chr2:37384328-37384329	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs12992818	chr2:37384362-37384363	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs12992610	chr2:37384383-37384384	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs113554883	chr2:37384430-37384431	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs7340267	chr2:37384460-37384461	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37312200-37383200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:37336400-37383200	Weak transcription	Psoas Muscle	Psoas
3	chr2:37355000-37383200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:37361800-37383200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr2:37365800-37383600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr2:37371200-37383200	Weak transcription	Colonic Mucosa	Colon
7	chr2:37372200-37383200	Weak transcription	Gastric	stomach
8	chr2:37372600-37383200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:37374400-37383200	Weak transcription	NH-A	brain
10	chr2:37375000-37383200	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr2:37375800-37383200	Weak transcription	Lung	lung
12	chr2:37377200-37383200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr2:37379800-37383200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr2:37380600-37383200	Weak transcription	Ovary	ovary
15	chr2:37381200-37383200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:37381200-37383200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr2:37381600-37383200	Enhancers	Primary B cells from peripheral blood	blood
18	chr2:37381600-37383200	Enhancers	Primary T cells fromperipheralblood	blood
19	chr2:37382000-37383200	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr2:37382000-37383200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr2:37382000-37383200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr2:37382200-37383200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr2:37382200-37383200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr2:37382200-37383200	Enhancers	Primary B cells from cord blood	blood
25	chr2:37382200-37383200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr2:37382200-37383200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr2:37382200-37383200	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr2:37382200-37383200	Enhancers	Right Atrium	heart
29	chr2:37382200-37383200	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr2:37382200-37383200	Enhancers	Spleen	Spleen
31	chr2:37382200-37383400	Flanking Active TSS	NHEK	skin
32	chr2:37382200-37383600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
33	chr2:37382200-37383600	Flanking Active TSS	Dnd41	blood
34	chr2:37382200-37383800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr2:37382400-37383200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr2:37382400-37383200	Enhancers	Liver	Liver
37	chr2:37382400-37383200	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr2:37382400-37383200	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr2:37382400-37383200	Enhancers	Stomach Mucosa	stomach
40	chr2:37382400-37383400	Flanking Active TSS	Brain Hippocampus Middle	brain
41	chr2:37382400-37383600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr2:37382400-37383800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
43	chr2:37382400-37383800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr2:37382600-37383200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:37382600-37383200	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr2:37382600-37383200	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr2:37382600-37383200	Enhancers	Brain Substantia Nigra	brain
48	chr2:37382600-37383200	Enhancers	Esophagus	oesophagus
49	chr2:37382600-37383200	Enhancers	Fetal Heart	heart
50	chr2:37382600-37383200	Enhancers	Fetal Lung	lung

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