Variant report

Variant	nsv1062441
Chromosome Location	chr20:23861343-23955100
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	BHLHE40	chr20:23909552-23909553	K562	blood:	n/a	n/a
2	BRCA1	chr20:23870442-23870605	HepG2	liver:	n/a	n/a
3	CEBPB	chr20:23934298-23934572	HepG2	liver:	n/a	chr20:23934424-23934435
4	CEBPB	chr20:23932569-23932853	A549	lung:	n/a	chr20:23932702-23932715 chr20:23932702-23932715 chr20:23932704-23932713 chr20:23932704-23932713 chr20:23932704-23932713 chr20:23932702-23932713 chr20:23932704-23932713 chr20:23932704-23932715
5	CEBPB	chr20:23900611-23901506	MCF-7	breast:	n/a	chr20:23901302-23901313
6	CEBPB	chr20:23934284-23934571	A549	lung:	n/a	chr20:23934424-23934435
7	CEBPB	chr20:23900626-23901487	MCF-7	breast:	n/a	chr20:23901302-23901313
8	CEBPB	chr20:23868265-23868462	HepG2	liver:	n/a	n/a
9	CEBPB	chr20:23901279-23901335	HepG2	liver:	n/a	chr20:23901302-23901313
10	CEBPB	chr20:23932543-23932848	HepG2	liver:	n/a	chr20:23932702-23932715 chr20:23932702-23932715 chr20:23932704-23932713 chr20:23932704-23932713 chr20:23932704-23932713 chr20:23932702-23932713 chr20:23932704-23932713 chr20:23932704-23932715
11	CEBPB	chr20:23932580-23932833	IMR90	lung:	n/a	chr20:23932702-23932715 chr20:23932702-23932715 chr20:23932704-23932713 chr20:23932704-23932713 chr20:23932704-23932713 chr20:23932702-23932713 chr20:23932704-23932713 chr20:23932704-23932715
12	CHD2	chr20:23870402-23870415	HepG2	liver:	n/a	n/a
13	CTCF	chr20:23918100-23918250	HAc	cerebellar:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144
14	CTCF	chr20:23870692-23870767	GM19240	blood:	n/a	n/a
15	CTCF	chr20:23917961-23918235	K562	blood:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
16	CTCF	chr20:23917991-23918227	ECC-1	luminal epithelium:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
17	CTCF	chr20:23918080-23918230	SAEC	small airway:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
18	CTCF	chr20:23870440-23870590	AG09309	skin:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
19	CTCF	chr20:23870440-23870590	GM12865	blood:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
20	CTCF	chr20:23918120-23918270	WERI-Rb-1	eye:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144
21	CTCF	chr20:23918020-23918170	NHEK	skin:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
22	CTCF	chr20:23917999-23918279	GM19240	blood:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
23	CTCF	chr20:23918060-23918210	WI-38	lung:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
24	CTCF	chr20:23870500-23870650	HAc	cerebellar:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
25	CTCF	chr20:23870480-23870630	HCT-116	colon:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
26	CTCF	chr20:23870460-23870610	HRE	kidney:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
27	CTCF	chr20:23870440-23870590	BE2_C	brain:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
28	CTCF	chr20:23917988-23918316	A549	lung:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
29	CTCF	chr20:23918060-23918210	AoAF	blood vessel:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
30	CTCF	chr20:23870440-23870590	GM12869	blood:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
31	CTCF	chr20:23870440-23870590	GM12875	blood:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
32	CTCF	chr20:23918100-23918250	WI-38	lung:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144
33	CTCF	chr20:23870440-23870590	AG09319	gingival:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
34	CTCF	chr20:23870440-23870590	AG10803	skin:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
35	CTCF	chr20:23870420-23870570	GM12872	blood:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
36	CTCF	chr20:23870711-23870820	Hela-S3	cervix:	n/a	chr20:23870761-23870779 chr20:23870762-23870778 chr20:23870808-23870817 chr20:23870763-23870784
37	CTCF	chr20:23870420-23870570	GM12864	blood:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
38	CTCF	chr20:23870355-23870644	LNCaP	prostate:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
39	CTCF	chr20:23870420-23870570	HCPEpiC	choroid plexus:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
40	CTCF	chr20:23917801-23917880	GM19238	blood:	n/a	n/a
41	CTCF	chr20:23918080-23918230	HPF	lung:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
42	CTCF	chr20:23917933-23918247	A549	lung:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
43	CTCF	chr20:23918019-23918270	Lung_OC	lung:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
44	CTCF	chr20:23917955-23918350	IMR90	lung:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
45	CTCF	chr20:23918060-23918210	NHDF-neo	bronchial:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108
46	CTCF	chr20:23870440-23870590	HCPEpiC	choroid plexus:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
47	CTCF	chr20:23870382-23870633	Kidney_OC	kidney:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
48	CTCF	chr20:23870440-23870590	Caco-2	colon:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
49	CTCF	chr20:23870440-23870590	GM12867	blood:	n/a	chr20:23870514-23870532 chr20:23870516-23870537 chr20:23870517-23870526
50	CTCF	chr20:23917973-23918302	Gliobla	brain:	n/a	chr20:23918134-23918155 chr20:23918132-23918150 chr20:23918135-23918144 chr20:23918095-23918108

No.	Distal block	Cell Line	Cell type
1	chr20:23917806..23918382-chr20:23976746..23977457,2	MCF-7	breast:
2	chr20:23648842..23649774-chr20:23870335..23871266,4	MCF-7	breast:
3	chr20:23945696..23947620-chr20:23948885..23951214,2	MCF-7	breast:
4	chr20:23918328..23919972-chr20:23977586..23980315,2	MCF-7	breast:
5	chr20:23870254..23870831-chr20:23976722..23977413,2	MCF-7	breast:
6	chr20:23870451..23870966-chr20:24081176..24081813,2	MCF-7	breast:
7	chr20:23895606..23897789-chr20:23899245..23901665,2	MCF-7	breast:
8	chr20:23895606..23897789-chr20:23899245..23901665,2	MCF-7	breast:
9	chr20:23870329..23871235-chr20:23976503..23977926,6	MCF-7	breast:
10	chr20:23917673..23918874-chr20:23976593..23977514,3	K562	blood:
11	chr20:23763057..23763763-chr20:23870036..23871243,3	MCF-7	breast:
12	chr20:23870354..23871060-chr20:23917733..23918317,2	MCF-7	breast:
13	chr20:23945696..23947620-chr20:23948885..23951214,2	MCF-7	breast:
14	chr20:23870354..23871060-chr20:23917733..23918317,2	MCF-7	breast:
15	chr20:23917874..23918575-chr20:24189095..24189921,2	MCF-7	breast:
16	chr20:23779854..23780390-chr20:23870001..23870554,2	MCF-7	breast:
17	chr20:23918077..23918602-chr20:24144722..24145283,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST5-1	chr20:23904588-23904694	NONHSAT079090
2	lnc-CST5-1	chr20:23909251-23909558	NONHSAT079090

Variant related genes	Relation type
CST5	TF binding region
CSTP1	TF binding region

Extended variants
information (count: 2448 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2448 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139551987	chr20:23861350-23861351	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs73902201	chr20:23861365-23861366	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs571810529	chr20:23861381-23861382	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs538394253	chr20:23861398-23861399	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs149977953	chr20:23861440-23861441	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs374763102	chr20:23861441-23861442	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs567687838	chr20:23861462-23861463	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs6114357	chr20:23861486-23861487	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs536616279	chr20:23861490-23861491	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs545435526	chr20:23861501-23861502	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs555410981	chr20:23861516-23861517	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs565940993	chr20:23861530-23861531	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs534561400	chr20:23861542-23861543	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs115384678	chr20:23861553-23861554	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs577374354	chr20:23861561-23861562	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs73610754	chr20:23861564-23861565	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs145263511	chr20:23861583-23861584	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs148735044	chr20:23861596-23861597	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs118086034	chr20:23861597-23861598	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs542591105	chr20:23861607-23861608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73902202	chr20:23861622-23861623	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs573475077	chr20:23861624-23861625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545676860	chr20:23861632-23861633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190147240	chr20:23861652-23861653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs377116019	chr20:23861669-23861670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571983079	chr20:23861677-23861678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142409726	chr20:23861702-23861703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561420330	chr20:23861704-23861705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4350819	chr20:23861705-23861706	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs113407581	chr20:23861713-23861714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565872318	chr20:23861732-23861733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561050939	chr20:23861775-23861776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551213816	chr20:23861805-23861806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571130744	chr20:23861833-23861834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536815450	chr20:23861849-23861850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147918214	chr20:23861872-23861873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372519217	chr20:23861876-23861877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374514835	chr20:23861923-23861924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs180986671	chr20:23861944-23861945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78565889	chr20:23861987-23861988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572703611	chr20:23862001-23862002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545740342	chr20:23862003-23862004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs73905803	chr20:23862031-23862032	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs141749868	chr20:23862034-23862035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368626841	chr20:23862042-23862043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371606500	chr20:23862043-23862044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4075883	chr20:23862056-23862057	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs546735090	chr20:23862057-23862058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73905804	chr20:23862076-23862077	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs6114358	chr20:23862123-23862124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23852400-23864800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr20:23858200-23862800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr20:23859200-23861800	Enhancers	Lung	lung
4	chr20:23859400-23861400	Enhancers	Placenta Amnion	Placenta Amnion
5	chr20:23859400-23862400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr20:23859800-23862400	Enhancers	Pancreas	Pancrea
7	chr20:23860000-23861600	Enhancers	Rectal Smooth Muscle	rectum
8	chr20:23860000-23862200	Enhancers	HepG2	liver
9	chr20:23860200-23861600	Enhancers	Fetal Intestine Large	intestine
10	chr20:23860400-23861400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
11	chr20:23860600-23861400	Enhancers	Fetal Lung	lung
12	chr20:23860600-23861600	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr20:23860600-23861600	Bivalent Enhancer	Fetal Stomach	stomach
14	chr20:23860600-23861800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr20:23860600-23862200	Enhancers	HMEC	breast
16	chr20:23860600-23862400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr20:23860800-23861800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr20:23860800-23862200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr20:23861000-23864600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr20:23861200-23861400	Flanking Active TSS	Stomach Smooth Muscle	stomach
21	chr20:23861200-23861800	Enhancers	NHEK	skin
22	chr20:23861400-23862200	Enhancers	Esophagus	oesophagus
23	chr20:23861400-23862400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr20:23861400-23864400	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr20:23861600-23861800	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr20:23861600-23862200	Enhancers	Placenta	Placenta
27	chr20:23861800-23862000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr20:23862200-23862400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr20:23862200-23862400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr20:23862200-23863800	Weak transcription	Placenta	Placenta
31	chr20:23862200-23866400	Weak transcription	Esophagus	oesophagus
32	chr20:23862400-23862800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr20:23862400-23863400	Weak transcription	Pancreas	Pancrea
34	chr20:23863400-23864200	Enhancers	Pancreas	Pancrea
35	chr20:23863800-23865400	Enhancers	Placenta	Placenta
36	chr20:23864400-23865400	Enhancers	Placenta Amnion	Placenta Amnion
37	chr20:23864600-23865400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr20:23864800-23865000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr20:23865400-23870400	Weak transcription	Placenta	Placenta
40	chr20:23866400-23866600	Enhancers	Esophagus	oesophagus
41	chr20:23866600-23870000	Weak transcription	Esophagus	oesophagus
42	chr20:23868000-23868400	Enhancers	Right Atrium	heart
43	chr20:23868000-23868600	Enhancers	Fetal Thymus	thymus
44	chr20:23868600-23870000	Weak transcription	Fetal Thymus	thymus
45	chr20:23870000-23870200	Enhancers	Esophagus	oesophagus
46	chr20:23870000-23870800	Enhancers	Fetal Thymus	thymus
47	chr20:23870200-23871000	Enhancers	Dnd41	blood
48	chr20:23870200-23871200	Enhancers	Primary T cells fromperipheralblood	blood
49	chr20:23870400-23870800	Enhancers	Placenta	Placenta
50	chr20:23870400-23871000	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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