Variant report

Variant	esv1803710
Chromosome Location	chr2:211073376-211173763
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	chr2:211113387-211113738	HepG2	liver:	n/a	chr2:211113389-211113405 chr2:211113390-211113406
2	BACH1	chr2:211089442-211089626	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:211089846-211090345	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr2:211117672-211117742	GM12878	blood:	n/a	n/a
5	CEBPB	chr2:211126182-211126488	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:211092536-211092704	H1-hESC	embryonic stem cell:	n/a	chr2:211092606-211092617
7	CEBPB	chr2:211092484-211092716	HepG2	liver:	n/a	chr2:211092606-211092617
8	CEBPB	chr2:211094725-211095046	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr2:211086349-211086750	Hela-S3	cervix:	n/a	chr2:211086508-211086519
10	CEBPB	chr2:211092133-211092295	A549	lung:	n/a	n/a
11	CEBPB	chr2:211086421-211086579	HepG2	liver:	n/a	chr2:211086508-211086519
12	CEBPB	chr2:211090100-211090474	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:211086359-211086634	H1-hESC	embryonic stem cell:	n/a	chr2:211086508-211086519
14	CEBPB	chr2:211086416-211086593	A549	lung:	n/a	chr2:211086508-211086519
15	CEBPB	chr2:211095414-211095499	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:211086356-211086629	HepG2	liver:	n/a	chr2:211086508-211086519
17	CEBPB	chr2:211087782-211088167	Hela-S3	cervix:	n/a	chr2:211087990-211088003 chr2:211087962-211087973
18	CEBPB	chr2:211086356-211086636	IMR90	lung:	n/a	chr2:211086508-211086519
19	CEBPB	chr2:211126127-211126519	MCF-7	breast:	n/a	n/a
20	CEBPB	chr2:211123613-211123956	HepG2	liver:	n/a	chr2:211123742-211123753
21	CEBPB	chr2:211153819-211154128	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:211123634-211123928	A549	lung:	n/a	chr2:211123742-211123753
23	CEBPB	chr2:211153891-211154063	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr2:211153833-211154120	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:211090942-211091595	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:211092491-211092679	HepG2	liver:	n/a	chr2:211092606-211092617
27	CEBPB	chr2:211087863-211088099	HepG2	liver:	n/a	chr2:211087990-211088003 chr2:211087962-211087973
28	CEBPB	chr2:211091957-211092751	Hela-S3	cervix:	n/a	chr2:211092606-211092617
29	CEBPB	chr2:211123715-211123833	H1-hESC	embryonic stem cell:	n/a	chr2:211123742-211123753
30	CEBPB	chr2:211092044-211092759	HepG2	liver:	n/a	chr2:211092606-211092617
31	CEBPB	chr2:211095822-211096042	HepG2	liver:	n/a	chr2:211095949-211095962 chr2:211095951-211095962 chr2:211095951-211095962 chr2:211095949-211095960
32	CEBPD	chr2:211092485-211092734	HepG2	liver:	n/a	n/a
33	CHD1	chr2:211089543-211090182	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr2:211089927-211090159	HepG2	liver:	n/a	n/a
35	CREB1	chr2:211089454-211090096	A549	lung:	n/a	n/a
36	CTBP2	chr2:211089443-211090226	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr2:211113500-211113650	HUVEC	blood vessel:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
38	CTCF	chr2:211113540-211113690	HCPEpiC	choroid plexus:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
39	CTCF	chr2:211113403-211113734	IMR90	lung:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
40	CTCF	chr2:211098380-211098530	HEK293	kidney:	n/a	n/a
41	CTCF	chr2:211089943-211089999	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr2:211113460-211113610	GM12872	blood:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
43	CTCF	chr2:211113270-211113869	HCT-116	colon:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
44	CTCF	chr2:211113500-211113650	SK-N-SH_RA	brain:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
45	CTCF	chr2:211113520-211113670	AG04449	skin:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
46	CTCF	chr2:211113453-211113676	Medullo	brain:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
47	CTCF	chr2:211169347-211169358	LNCaP	prostate:	n/a	n/a
48	CTCF	chr2:211090080-211090230	HRE	kidney:	n/a	n/a
49	CTCF	chr2:211113466-211113656	Pancreas_OC	pancreas:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
50	CTCF	chr2:211090111-211090205	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:211096859-211096909	AG04450	lung:	fetal
2	chr2:211096859-211096909	AoSMC	blood vessel:	n/a
3	chr2:211096859-211096909	AG04450	lung:	fetal
4	chr2:211096859-211096909	AoSMC	blood vessel:	n/a
5	chr2:211089815-211089865	MCF-7	breast:	n/a
6	chr2:211093895-211093945	ovcar-3	ovarian:	n/a
7	chr2:211091510-211091560	HCT-116	colon:	n/a
8	chr2:211096347-211096397	HepG2	liver:	n/a
9	chr2:211090117-211090167	Hepatocyte	liver:	n/a
10	chr2:211096859-211096909	SKMC	muscle:	n/a
11	chr2:211155085-211155135	HEEpiC	esophagus:	n/a
12	chr2:211090349-211090399	HRE	kidney:	n/a
13	chr2:211096859-211096909	NHBE	bronchial:	n/a
14	chr2:211090487-211090537	GM12878	blood:	n/a
15	chr2:211089815-211089865	BJ	skin:	n/a
16	chr2:211090117-211090167	SK-N-MC	brain:	n/a
17	chr2:211090271-211090321	GM12878	blood:	n/a
18	chr2:211090281-211090331	A549	lung:	n/a
19	chr2:211096859-211096909	HEK293	kidney:	embryo
20	chr2:211090117-211090167	HMEC	breast:	n/a
21	chr2:211090171-211090221	GM12891	blood:	n/a
22	chr2:211090117-211090167	NH-A	brain:	n/a
23	chr2:211090281-211090331	HCM	heart:	n/a
24	chr2:211090349-211090399	HCPEpiC	choroid plexus:	n/a
25	chr2:211090281-211090331	CMK	blood:	n/a
26	chr2:211090487-211090537	U87	brain:	n/a
27	chr2:211090117-211090167	HAEpiC	amniotic membrane:	n/a
28	chr2:211168547-211168597	HCPEpiC	choroid plexus:	n/a
29	chr2:211091510-211091560	Hela-S3	cervix:	n/a
30	chr2:211090171-211090221	PANC-1	pancreas:	n/a
31	chr2:211096859-211096909	GM06990	blood:	n/a
32	chr2:211169638-211169688	NH-A	brain:	n/a
33	chr2:211089815-211089865	HMEC	breast:	n/a
34	chr2:211090487-211090537	HL-60	blood:	n/a
35	chr2:211090271-211090321	HL-60	blood:	n/a
36	chr2:211091510-211091560	SKMC	muscle:	n/a
37	chr2:211091510-211091560	HCPEpiC	choroid plexus:	n/a
38	chr2:211090487-211090537	NB4	blood:	n/a
39	chr2:211155085-211155135	MCF-7	breast:	n/a
40	chr2:211096347-211096397	K562	blood:	n/a
41	chr2:211090323-211090373	HEEpiC	esophagus:	n/a
42	chr2:211093895-211093945	NH-A	brain:	n/a
43	chr2:211093895-211093945	MCF10A-Er-Src	breast:	n/a
44	chr2:211090171-211090221	Jurkat	blood:	n/a
45	chr2:211169638-211169688	H1-hESC	embryonic stem cell:	embryo
46	chr2:211091510-211091560	LNCaP	prostate:	n/a
47	chr2:211089678-211089728	U87	brain:	n/a
48	chr2:211090281-211090331	NHDF-neo	bronchial:	n/a
49	chr2:211089678-211089728	SK-N-MC	brain:	n/a
50	chr2:211091510-211091560	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:41465713..41467651-chr2:211089515..211091035,2	K562	blood:
2	chr2:211082052..211083888-chr2:211086942..211089346,2	K562	blood:
3	chr2:211106656..211109050-chr2:211112844..211114921,2	K562	blood:
4	chr2:211128325..211129018-chr2:211137774..211138284,2	MCF-7	breast:
5	chr17:41463157..41466155-chr2:211088015..211089515,2	K562	blood:
6	chr17:41466368..41468065-chr2:211089535..211091035,2	K562	blood:
7	chr2:211173735..211175248-chr2:211176739..211178731,2	MCF-7	breast:
8	chr2:211078316..211079872-chr2:211083678..211086090,2	MCF-7	breast:
9	chr2:211128325..211129018-chr2:211137774..211138284,2	MCF-7	breast:
10	chr17:41464702..41466633-chr2:211088015..211091015,4	MCF-7	breast:
11	chr2:211082052..211083888-chr2:211086942..211089346,2	K562	blood:
12	chr2:211106656..211109050-chr2:211112844..211114921,2	K562	blood:
13	chr12:124746104..124746706-chr2:211100326..211100835,2	MCF-7	breast:
14	chr2:211113028..211114042-chr2:211263878..211264898,6	MCF-7	breast:
15	chr2:211078316..211079872-chr2:211083678..211086090,2	MCF-7	breast:
16	chr2:211112989..211113918-chr2:211900038..211900547,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2orf67-2	chr2:211082789-211082826	NONHSAT076675
2	lnc-C2orf67-2	chr2:211085371-211085526	NONHSAT076675
3	lnc-RPE-9	chr2:211097416-211098700	NONHSAT076676
4	lnc-RPE-2	chr2:211083196-211083288	ENSG00000231294.1
5	lnc-C2orf67-2	chr2:211089039-211089573	NONHSAT076675
6	lnc-RPE-2	chr2:211095007-211095107	ENSG00000231294.1

Variant related genes	Relation type
ACADL	TF binding region
ENSG00000199203	TF binding region
MYL1	TF binding region
ACADL	CpG island
ENSG00000199203	CpG island
MYL1	CpG island
ENSG00000188825	chromatin interactions

Extended variants
information (count: 1979 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1979 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10172429	chr2:211073376-211073377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549267276	chr2:211073397-211073398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572374438	chr2:211073434-211073435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546088429	chr2:211073440-211073441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371319987	chr2:211073446-211073447	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541594322	chr2:211073458-211073459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565892345	chr2:211073514-211073515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528674376	chr2:211073531-211073532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564297368	chr2:211073535-211073536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78385875	chr2:211073545-211073546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1509571	chr2:211073548-211073549	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs536779776	chr2:211073549-211073550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144117914	chr2:211073624-211073625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567198988	chr2:211073642-211073643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561948452	chr2:211073726-211073727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182675793	chr2:211073741-211073742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553314223	chr2:211073811-211073812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187849532	chr2:211073812-211073813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545249042	chr2:211073888-211073889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558500170	chr2:211073905-211073906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575684990	chr2:211073920-211073921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs59610629	chr2:211074008-211074009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543596788	chr2:211074009-211074010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563651186	chr2:211074065-211074066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35537244	chr2:211074068-211074069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs56301246	chr2:211074097-211074098	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs76522766	chr2:211074263-211074264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542876689	chr2:211074302-211074303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376547441	chr2:211074328-211074329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559640660	chr2:211074329-211074330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529387528	chr2:211074408-211074409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528786765	chr2:211074443-211074444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113637570	chr2:211074464-211074465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191996357	chr2:211074484-211074485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111760491	chr2:211074634-211074635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183222311	chr2:211074663-211074664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561661792	chr2:211074706-211074707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530628263	chr2:211074822-211074823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369461871	chr2:211074873-211074874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374168844	chr2:211074877-211074878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs3764913	chr2:211074909-211074910	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
42	rs369064648	chr2:211075006-211075007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368935556	chr2:211075026-211075027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536270350	chr2:211075053-211075054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546890985	chr2:211075130-211075131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150232893	chr2:211075146-211075147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1509570	chr2:211075202-211075203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs375813056	chr2:211075213-211075214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138896241	chr2:211075236-211075237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369481020	chr2:211075256-211075257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	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
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211051000-211086600	Weak transcription	Adipose Nuclei	Adipose
2	chr2:211052200-211085600	Weak transcription	Aorta	Aorta
3	chr2:211060200-211086600	Weak transcription	Pancreas	Pancrea
4	chr2:211060400-211078600	Weak transcription	Fetal Muscle Leg	muscle
5	chr2:211060400-211089000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr2:211067800-211089200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr2:211068200-211073400	Weak transcription	Liver	Liver
8	chr2:211072200-211080000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr2:211073400-211075000	Strong transcription	Liver	Liver
10	chr2:211075000-211080200	Weak transcription	Liver	Liver
11	chr2:211079400-211079800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:211079400-211080400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:211079400-211080600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr2:211079600-211080400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr2:211079600-211080400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr2:211079800-211080200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr2:211079800-211080200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr2:211079800-211080400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr2:211079800-211080600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:211080000-211080200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr2:211080000-211080200	Enhancers	Gastric	stomach
22	chr2:211080000-211080400	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr2:211080000-211080400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr2:211080200-211084200	Strong transcription	Liver	Liver
25	chr2:211080200-211089400	Weak transcription	Gastric	stomach
26	chr2:211080400-211081000	Enhancers	Fetal Kidney	kidney
27	chr2:211084200-211086600	Weak transcription	Liver	Liver
28	chr2:211085600-211087400	Enhancers	Aorta	Aorta
29	chr2:211086600-211086800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:211086600-211087600	Enhancers	Pancreas	Pancrea
31	chr2:211086600-211088200	Enhancers	Liver	Liver
32	chr2:211086600-211088400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr2:211086600-211088600	Enhancers	Adipose Nuclei	Adipose
34	chr2:211086800-211087600	Enhancers	Placenta	Placenta
35	chr2:211086800-211087800	Enhancers	Hela-S3	cervix
36	chr2:211087400-211087600	Flanking Active TSS	Aorta	Aorta
37	chr2:211087400-211087600	Bivalent Enhancer	HepG2	liver
38	chr2:211087600-211088600	Weak transcription	Pancreas	Pancrea
39	chr2:211087600-211091000	Active TSS	Aorta	Aorta
40	chr2:211087800-211088000	Bivalent Enhancer	Fetal Lung	lung
41	chr2:211087800-211090200	Weak transcription	Hela-S3	cervix
42	chr2:211088200-211088400	Flanking Active TSS	Liver	Liver
43	chr2:211088400-211088600	Enhancers	Liver	Liver
44	chr2:211088400-211089200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:211088600-211088800	Flanking Active TSS	Adipose Nuclei	Adipose
46	chr2:211088600-211088800	Flanking Active TSS	Liver	Liver
47	chr2:211088600-211090600	Active TSS	Pancreas	Pancrea
48	chr2:211088800-211089000	Enhancers	Liver	Liver
49	chr2:211088800-211089400	Active TSS	Adipose Nuclei	Adipose
50	chr2:211088800-211090600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell

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