Variant report

Variant	esv3356302
Chromosome Location	chr2:183962495-183989877
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	ARID3A	chr2:183988933-183990031	K562	blood:	n/a	n/a
2	ARID3A	chr2:183988399-183989979	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:183977385-183977757	K562	blood:	n/a	n/a
4	ARID3A	chr2:183977968-183978126	K562	blood:	n/a	n/a
5	ATF1	chr2:183988548-183989798	K562	blood:	n/a	n/a
6	ATF1	chr2:183977365-183977711	K562	blood:	n/a	n/a
7	ATF2	chr2:183988711-183989839	GM12878	blood:	n/a	n/a
8	ATF2	chr2:183988667-183989691	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr2:183989322-183989822	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr2:183988604-183989274	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr2:183988645-183989273	GM12878	blood:	n/a	n/a
12	ATF3	chr2:183988652-183989324	K562	blood:	n/a	n/a
13	ATF3	chr2:183988586-183989641	A549	lung:	n/a	n/a
14	ATF3	chr2:183988781-183989391	A549	lung:	n/a	n/a
15	BACH1	chr2:183977993-183978041	K562	blood:	n/a	n/a
16	BACH1	chr2:183970245-183970405	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr2:183989459-183989903	GM12878	blood:	n/a	n/a
18	BCL3	chr2:183988433-183989951	A549	lung:	n/a	n/a
19	BCL3	chr2:183988569-183989937	A549	lung:	n/a	n/a
20	BCLAF1	chr2:183988851-183989956	GM12878	blood:	n/a	n/a
21	BHLHE40	chr2:183970227-183970519	K562	blood:	n/a	n/a
22	BHLHE40	chr2:183988338-183990089	K562	blood:	n/a	n/a
23	BHLHE40	chr2:183988760-183989787	HepG2	liver:	n/a	n/a
24	BHLHE40	chr2:183988768-183990091	GM12878	blood:	n/a	n/a
25	BRCA1	chr2:183988798-183989217	HepG2	liver:	n/a	n/a
26	BRCA1	chr2:183989470-183989911	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr2:183989428-183989792	HepG2	liver:	n/a	n/a
28	BRCA1	chr2:183989056-183989582	GM12878	blood:	n/a	n/a
29	CBX3	chr2:183988654-183990007	K562	blood:	n/a	chr2:183988684-183988695
30	CBX3	chr2:183988322-183989979	K562	blood:	n/a	chr2:183988684-183988695
31	CBX3	chr2:183977286-183977770	K562	blood:	n/a	n/a
32	CCNT2	chr2:183988425-183988645	K562	blood:	n/a	n/a
33	CCNT2	chr2:183989031-183989715	K562	blood:	n/a	n/a
34	CCNT2	chr2:183977433-183977679	K562	blood:	n/a	n/a
35	CEBPB	chr2:183988831-183989316	K562	blood:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
36	CEBPB	chr2:183988723-183989814	IMR90	lung:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
37	CEBPB	chr2:183988817-183989355	HepG2	liver:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
38	CEBPB	chr2:183970285-183970372	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:183988871-183989343	A549	lung:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
40	CEBPB	chr2:183988812-183989563	HepG2	liver:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
41	CEBPB	chr2:183988770-183989414	MCF-7	breast:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
42	CEBPB	chr2:183988912-183989192	HepG2	liver:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
43	CEBPB	chr2:183988850-183989332	ECC-1	luminal epithelium:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
44	CEBPB	chr2:183988715-183989367	ECC-1	luminal epithelium:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
45	CEBPB	chr2:183988536-183989866	HCT-116	colon:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
46	CEBPB	chr2:183988852-183989755	HepG2	liver:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
47	CEBPB	chr2:183988721-183989810	A549	lung:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
48	CEBPB	chr2:183988606-183990147	K562	blood:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
49	CEBPB	chr2:183988456-183989689	GM12878	blood:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089
50	CEBPB	chr2:183988608-183989891	HCT-116	colon:	n/a	chr2:183989080-183989089 chr2:183989080-183989089 chr2:183989078-183989091 chr2:183989080-183989089

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183988933-183988983	U87	brain:	n/a
2	chr2:183989107-183989157	MCF10A-Er-Src	breast:	n/a
3	chr2:183988933-183988983	HMEC	breast:	n/a
4	chr2:183988872-183988922	ProgFib	skin:	n/a
5	chr2:183988872-183988922	HMEC	breast:	n/a
6	chr2:183989067-183989117	CMK	blood:	n/a
7	chr2:183989218-183989268	PrEC	prostate:	n/a
8	chr2:183988933-183988983	HCPEpiC	choroid plexus:	n/a
9	chr2:183988968-183989018	BJ	skin:	n/a
10	chr2:183988000-183988050	SKMC	muscle:	n/a
11	chr2:183988000-183988050	AoSMC	blood vessel:	n/a
12	chr2:183989107-183989157	HNPCEpiC	eye:	n/a
13	chr2:183988872-183988922	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:183988968-183989018	SK-N-MC	brain:	n/a
15	chr2:183989047-183989097	RPTEC	kidney:	n/a
16	chr2:183989548-183989598	AG09319	gingival:	n/a
17	chr2:183989047-183989097	HNPCEpiC	eye:	n/a
18	chr2:183989548-183989598	HRE	kidney:	n/a
19	chr2:183988960-183989010	PANC-1	pancreas:	n/a
20	chr2:183988933-183988983	LNCaP	prostate:	n/a
21	chr2:183988933-183988983	PANC-1	pancreas:	n/a
22	chr2:183963421-183963471	MCF10A-Er-Src	breast:	n/a
23	chr2:183988960-183989010	AoSMC	blood vessel:	n/a
24	chr2:183988000-183988050	NT2-D1	testis:	n/a
25	chr2:183989067-183989117	K562	blood:	n/a
26	chr2:183988933-183988983	K562	blood:	n/a
27	chr2:183988960-183989010	AG04450	lung:	fetal
28	chr2:183989218-183989268	PFSK-1	brain:	n/a
29	chr2:183988933-183988983	NH-A	brain:	n/a
30	chr2:183989218-183989268	SK-N-MC	brain:	n/a
31	chr2:183988960-183989010	SAEC	small airway:	n/a
32	chr2:183988000-183988050	CMK	blood:	n/a
33	chr2:183989548-183989598	LNCaP	prostate:	n/a
34	chr2:183963421-183963471	HL-60	blood:	n/a
35	chr2:183989067-183989117	BJ	skin:	n/a
36	chr2:183988933-183988983	SK-N-SH_RA	brain:	n/a
37	chr2:183988960-183989010	ECC-1	luminal epithelium:	n/a
38	chr2:183963421-183963471	K562	blood:	n/a
39	chr2:183989218-183989268	HRCEpiC	kidney:	n/a
40	chr2:183989218-183989268	SK-N-SH_RA	brain:	n/a
41	chr2:183988872-183988922	HUVEC	blood vessel:	n/a
42	chr2:183989067-183989117	AG04450	lung:	fetal
43	chr2:183988000-183988050	A549	lung:	n/a
44	chr2:183989107-183989157	HRPEpiC	eye:	n/a
45	chr2:183988968-183989018	HMEC	breast:	n/a
46	chr2:183989067-183989117	NT2-D1	testis:	n/a
47	chr2:183963421-183963471	HCT-116	colon:	n/a
48	chr2:183988872-183988922	ovcar-3	ovarian:	n/a
49	chr2:183988872-183988922	IMR90	lung:	fetal
50	chr2:183989067-183989117	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:183977949..183985615-chr2:183986503..183991971,13	K562	blood:
2	chr2:183942606..183944610-chr2:183988840..183990429,2	K562	blood:
3	chr2:183961564..183963218-chr2:183968375..183970375,2	K562	blood:
4	chr2:183989265..183990800-chr2:184010673..184012208,2	MCF-7	breast:
5	chr2:183902160..183905711-chr2:183988105..183989833,3	MCF-7	breast:
6	chr2:183967945..183970518-chr2:183975860..183978004,2	K562	blood:
7	chr2:182755789..182757861-chr2:183988319..183990505,2	K562	blood:
8	chr2:183981717..183985228-chr2:183986533..183989454,4	MCF-7	breast:
9	chr2:183941058..183944169-chr2:183988077..183990587,3	MCF-7	breast:
10	chr2:183981717..183985228-chr2:183986533..183989454,4	MCF-7	breast:
11	chr2:183977949..183985615-chr2:183986503..183991971,13	K562	blood:
12	chr2:183977930..183980927-chr2:183984054..183985620,2	MCF-7	breast:
13	chr2:183976023..183978343-chr2:183982634..183984997,2	K562	blood:
14	chr2:183961564..183963218-chr2:183968375..183970375,2	K562	blood:
15	chr2:183901632..183905004-chr2:183977592..183981292,4	K562	blood:
16	chr2:183836718..183838459-chr2:183989290..183991920,2	K562	blood:
17	chr2:183900414..183906188-chr2:183987961..183990917,10	MCF-7	breast:
18	chr2:183942521..183944578-chr2:183980527..183982888,2	K562	blood:
19	chr2:183989189..183990903-chr2:184002119..184004777,2	MCF-7	breast:
20	chr2:183975767..183977523-chr2:183982555..183984134,2	K562	blood:
21	chr2:183976023..183978343-chr2:183982634..183984997,2	K562	blood:
22	chr17:7475914..7477152-chr2:183988526..183989842,3	Hela-S3	cervix:
23	chr2:183897885..183903273-chr2:183986817..183992325,13	K562	blood:
24	chr2:183886816..183889401-chr2:183988651..183990376,2	K562	blood:
25	chr2:183970085..183972201-chr2:183987942..183989595,2	MCF-7	breast:
26	chr2:183977930..183980927-chr2:183984054..183985620,2	MCF-7	breast:
27	chr2:183975767..183977523-chr2:183982555..183984134,2	K562	blood:
28	chr2:183973630..183975717-chr2:183987994..183990316,2	K562	blood:
29	chr2:183895298..183904606-chr2:183986062..183992067,16	K562	blood:
30	chr2:183967945..183970518-chr2:183975860..183978004,2	K562	blood:
31	chr2:183942219..183944106-chr2:183988840..183990406,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NCKAP1-1	chr2:183973168-183973247	ENSG00000224643.1
2	lnc-DUSP19-1	chr2:183983319-183983667	NONHSAT075936
3	lnc-DUSP19-1	chr2:183982247-183982354	NONHSAT075936
4	lnc-DUSP19-1	chr2:183982268-183982354	XLOC_001778
5	lnc-NCKAP1-1	chr2:183972220-183972431	ENSG00000224643.1
6	lnc-DUSP19-1	chr2:183983319-183983470	XLOC_001778
7	lnc-DUSP19-1	chr2:183984734-183984790	NONHSAT075936

Variant related genes	Relation type
NUP35	TF binding region
ENSG00000224643	TF binding region
NUP35	CpG island
ENSG00000224643	CpG island
ENSG00000161960	chromatin interactions
ENSG00000163002	chromatin interactions
ENSG00000202141	chromatin interactions
ENSG00000138434	chromatin interactions
ENSG00000260742	chromatin interactions
ENSG00000162999	chromatin interactions
ENSG00000061676	chromatin interactions

Extended variants
information (count: 1042 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568802229	chr2:183962562-183962563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs187861491	chr2:183962663-183962664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147242520	chr2:183962680-183962681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574168215	chr2:183962693-183962694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536464895	chr2:183962701-183962702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553178377	chr2:183962710-183962711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191214987	chr2:183962750-183962751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201690998	chr2:183962793-183962794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545333137	chr2:183962815-183962816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565532646	chr2:183962848-183962849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575551328	chr2:183962854-183962855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140863214	chr2:183962869-183962870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184165295	chr2:183962870-183962871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530249811	chr2:183962919-183962920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547097296	chr2:183963009-183963010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560439470	chr2:183963023-183963024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532340090	chr2:183963074-183963075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552199838	chr2:183963100-183963101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569087103	chr2:183963171-183963172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72890381	chr2:183963186-183963187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78117021	chr2:183963260-183963261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567703133	chr2:183963285-183963286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533686454	chr2:183963301-183963302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2138485	chr2:183963330-183963331	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs144672228	chr2:183963421-183963422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373857960	chr2:183963422-183963423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559007668	chr2:183963491-183963492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575859405	chr2:183963659-183963660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2705730	chr2:183963690-183963691	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs555028346	chr2:183963713-183963714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550462681	chr2:183963742-183963743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574885714	chr2:183963768-183963769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs199916097	chr2:183963778-183963779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34335944	chr2:183963779-183963780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571807058	chr2:183963780-183963781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs397778401	chr2:183963788-183963789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74888232	chr2:183963800-183963801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189542945	chr2:183963811-183963812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560532628	chr2:183963829-183963830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532352909	chr2:183963832-183963833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545951562	chr2:183963842-183963843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562658231	chr2:183963853-183963854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531666400	chr2:183963948-183963949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548166628	chr2:183963959-183963960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369114133	chr2:183963964-183963965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550779831	chr2:183963975-183963976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs17704934	chr2:183963987-183963988	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs527250991	chr2:183963994-183963995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547092005	chr2:183964046-183964047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs72890384	chr2:183964067-183964068	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183944600-183963200	Weak transcription	Brain Angular Gyrus	brain
2	chr2:183944800-183962800	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr2:183945000-183962600	Weak transcription	Brain Hippocampus Middle	brain
4	chr2:183945000-183963400	Weak transcription	Fetal Intestine Small	intestine
5	chr2:183945000-183963400	Weak transcription	Fetal Stomach	stomach
6	chr2:183945600-183964000	Weak transcription	Colon Smooth Muscle	Colon
7	chr2:183945800-183972600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr2:183947000-183962800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr2:183947000-183963600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr2:183953200-183963600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr2:183954600-183988400	Weak transcription	Aorta	Aorta
12	chr2:183956000-183963600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr2:183956400-183963200	Weak transcription	Ovary	ovary
14	chr2:183958000-183963600	Weak transcription	Adipose Nuclei	Adipose
15	chr2:183959400-183970200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr2:183959800-183962800	Weak transcription	Small Intestine	intestine
17	chr2:183968200-183970600	Enhancers	Muscle Satellite Cultured Cells	--
18	chr2:183969800-183970800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:183969800-183970800	Enhancers	Hela-S3	cervix
20	chr2:183969800-183971000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr2:183970000-183970600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:183970000-183970600	Enhancers	HMEC	breast
23	chr2:183970000-183970600	Enhancers	HSMM	muscle
24	chr2:183970000-183970800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr2:183970000-183970800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:183970000-183970800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr2:183970000-183971000	Enhancers	A549	lung
28	chr2:183970200-183970600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr2:183970200-183970600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr2:183970200-183970600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr2:183970200-183970600	Enhancers	K562	blood
32	chr2:183970200-183970600	Enhancers	NHEK	skin
33	chr2:183970200-183970800	Enhancers	NHDF-Ad	bronchial
34	chr2:183976800-183977200	Enhancers	K562	blood
35	chr2:183977200-183978200	Flanking Active TSS	K562	blood
36	chr2:183978200-183979800	Enhancers	K562	blood
37	chr2:183982200-183982400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr2:183982400-183983600	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr2:183983200-183983600	Enhancers	HepG2	liver
40	chr2:183983600-183984400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr2:183983600-183984400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr2:183983600-183988200	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr2:183984200-183984400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:183984400-183988200	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr2:183984400-183988400	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr2:183986600-183988200	Weak transcription	Fetal Kidney	kidney
47	chr2:183987800-183988000	Bivalent/Poised TSS	Primary B cells from cord blood	blood
48	chr2:183987800-183988000	Weak transcription	K562	blood
49	chr2:183987800-183988200	Enhancers	HepG2	liver
50	chr2:183987800-183989600	Active TSS	Liver	Liver

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