Variant report

Variant	esv3437833
Chromosome Location	chr1:226780025-226810577
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:399)
CpG islands
(count:183)
Chromatin interactive
region (count:24)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:399 , 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	BATF	chr1:226810311-226810491	GM12878	blood:	n/a	n/a
2	BHLHE40	chr1:226796495-226796642	HepG2	liver:	n/a	n/a
3	BHLHE40	chr1:226796503-226796683	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:226790619-226790820	HepG2	liver:	n/a	n/a
5	BHLHE40	chr1:226796628-226796724	K562	blood:	n/a	n/a
6	CEBPB	chr1:226790428-226790703	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:226794164-226794280	K562	blood:	n/a	n/a
8	CTCF	chr1:226796540-226796690	GM12870	blood:	n/a	n/a
9	CTCF	chr1:226796320-226796470	HEEpiC	esophagus:	n/a	n/a
10	CTCF	chr1:226795880-226796030	GM12874	blood:	n/a	n/a
11	CTCF	chr1:226796520-226796670	GM12875	blood:	n/a	n/a
12	CTCF	chr1:226796580-226796730	HFF	foreskin:	n/a	n/a
13	CTCF	chr1:226796320-226796402	GM19240	blood:	n/a	n/a
14	CTCF	chr1:226790180-226790330	HPF	lung:	n/a	n/a
15	CTCF	chr1:226796492-226796732	ProgFib	skin:	n/a	n/a
16	CTCF	chr1:226796560-226796710	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr1:226799220-226799370	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr1:226796540-226796690	GM12873	blood:	n/a	n/a
19	CTCF	chr1:226796560-226796710	AG04449	skin:	n/a	n/a
20	CTCF	chr1:226796518-226796728	MCF-7	breast:	n/a	n/a
21	CTCF	chr1:226796500-226796650	HVMF	connective:	n/a	n/a
22	CTCF	chr1:226784599-226784792	K562	blood:	n/a	chr1:226784702-226784715
23	CTCF	chr1:226796920-226797070	GM12866	blood:	n/a	n/a
24	CTCF	chr1:226796434-226796688	ECC-1	luminal epithelium:	n/a	n/a
25	CTCF	chr1:226796560-226796710	GM12801	blood:	n/a	n/a
26	CTCF	chr1:226796520-226796670	GM12873	blood:	n/a	n/a
27	CTCF	chr1:226796540-226796690	SAEC	small airway:	n/a	n/a
28	CTCF	chr1:226784580-226784730	GM12872	blood:	n/a	chr1:226784702-226784715
29	CTCF	chr1:226799240-226799390	HMF	breast:	n/a	n/a
30	CTCF	chr1:226799262-226799303	ProgFib	skin:	n/a	n/a
31	CTCF	chr1:226796442-226796737	GM12892	blood:	n/a	n/a
32	CTCF	chr1:226784720-226784870	GM06990	blood:	n/a	n/a
33	CTCF	chr1:226784514-226784849	K562	blood:	n/a	chr1:226784702-226784715
34	CTCF	chr1:226784635-226784763	GM19238	blood:	n/a	chr1:226784702-226784715
35	CTCF	chr1:226796560-226796710	HEK293	kidney:	n/a	n/a
36	CTCF	chr1:226784680-226784830	GM12864	blood:	n/a	chr1:226784702-226784715
37	CTCF	chr1:226792400-226792550	Caco-2	colon:	n/a	n/a
38	CTCF	chr1:226796504-226796506	GM20000	blood:	n/a	n/a
39	CTCF	chr1:226799180-226799330	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr1:226796487-226796738	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:226796520-226796670	BE2_C	brain:	n/a	n/a
42	CTCF	chr1:226796479-226796723	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr1:226784672-226784776	H1-hESC	embryonic stem cell:	n/a	chr1:226784702-226784715
44	CTCF	chr1:226799080-226799230	NHEK	skin:	n/a	n/a
45	CTCF	chr1:226796492-226796761	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr1:226796860-226797010	GM12864	blood:	n/a	n/a
47	CTCF	chr1:226796540-226796690	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr1:226796378-226796851	HCT-116	colon:	n/a	n/a
49	CTCF	chr1:226796160-226796310	HMEC	breast:	n/a	n/a
50	CTCF	chr1:226796481-226796707	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:226795085-226795135	SK-N-MC	brain:	n/a
2	chr1:226792795-226792845	GM19239	blood:	n/a
3	chr1:226795085-226795135	Hela-S3	cervix:	n/a
4	chr1:226792795-226792845	NH-A	brain:	n/a
5	chr1:226795085-226795135	HIPEpiC	eye:	n/a
6	chr1:226795085-226795135	HCM	heart:	n/a
7	chr1:226792795-226792845	PrEC	prostate:	n/a
8	chr1:226792795-226792845	HCF	heart:	n/a
9	chr1:226791447-226791497	AoSMC	blood vessel:	n/a
10	chr1:226795085-226795135	T-47D	breast:	n/a
11	chr1:226792795-226792845	HIPEpiC	eye:	n/a
12	chr1:226791447-226791497	HEEpiC	esophagus:	n/a
13	chr1:226795085-226795135	AoSMC	blood vessel:	n/a
14	chr1:226792795-226792845	Hela-S3	cervix:	n/a
15	chr1:226792795-226792845	HRPEpiC	eye:	n/a
16	chr1:226792795-226792845	Jurkat	blood:	n/a
17	chr1:226795085-226795135	RPTEC	kidney:	n/a
18	chr1:226795085-226795135	K562	blood:	n/a
19	chr1:226791447-226791497	SK-N-SH	brain:	n/a
20	chr1:226795085-226795135	HEK293	kidney:	embryo
21	chr1:226791447-226791497	H1-hESC	embryonic stem cell:	embryo
22	chr1:226791447-226791497	HNPCEpiC	eye:	n/a
23	chr1:226791447-226791497	CMK	blood:	n/a
24	chr1:226791447-226791497	ovcar-3	ovarian:	n/a
25	chr1:226792795-226792845	GM12878	blood:	n/a
26	chr1:226791447-226791497	NH-A	brain:	n/a
27	chr1:226792795-226792845	RPTEC	kidney:	n/a
28	chr1:226795085-226795135	A549	lung:	n/a
29	chr1:226792795-226792845	PFSK-1	brain:	n/a
30	chr1:226795085-226795135	ProgFib	skin:	n/a
31	chr1:226792795-226792845	SAEC	small airway:	n/a
32	chr1:226791447-226791497	U87	brain:	n/a
33	chr1:226792795-226792845	NHDF-neo	bronchial:	n/a
34	chr1:226791447-226791497	Jurkat	blood:	n/a
35	chr1:226795085-226795135	H1-hESC	embryonic stem cell:	embryo
36	chr1:226795085-226795135	GM19239	blood:	n/a
37	chr1:226791447-226791497	SAEC	small airway:	n/a
38	chr1:226791447-226791497	HMEC	breast:	n/a
39	chr1:226792795-226792845	LNCaP	prostate:	n/a
40	chr1:226795085-226795135	NHDF-neo	bronchial:	n/a
41	chr1:226792795-226792845	HEEpiC	esophagus:	n/a
42	chr1:226792795-226792845	HCT-116	colon:	n/a
43	chr1:226791447-226791497	HRPEpiC	eye:	n/a
44	chr1:226795085-226795135	AG09319	gingival:	n/a
45	chr1:226792795-226792845	BJ	skin:	n/a
46	chr1:226792795-226792845	IMR90	lung:	fetal
47	chr1:226795085-226795135	ovcar-3	ovarian:	n/a
48	chr1:226792795-226792845	HMEC	breast:	n/a
49	chr1:226795085-226795135	PrEC	prostate:	n/a
50	chr1:226792795-226792845	HNPCEpiC	eye:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:226781867..226783443-chr1:226785494..226787232,2	K562	blood:
2	chr1:226770710..226772918-chr1:226790123..226792228,2	MCF-7	breast:
3	chr1:226589383..226591665-chr1:226794295..226796050,2	K562	blood:
4	chr1:226784697..226787234-chr1:226790961..226792707,2	MCF-7	breast:
5	chr1:226612138..226612852-chr1:226796151..226796974,3	MCF-7	breast:
6	chr1:226789700..226791399-chr1:226794121..226795784,2	K562	blood:
7	chr1:226787500..226789120-chr1:226793109..226795221,2	K562	blood:
8	chr1:226796572..226799349-chr1:227127668..227129647,2	K562	blood:
9	chr1:226784697..226787234-chr1:226790961..226792707,2	MCF-7	breast:
10	chr1:226779023..226781177-chr1:226804892..226807313,2	K562	blood:
11	chr1:226789700..226791399-chr1:226794121..226795784,2	K562	blood:
12	chr1:226796156..226797166-chr1:226813911..226814774,3	K562	blood:
13	chr1:226796607..226797490-chr1:226821558..226822493,2	K562	blood:
14	chr1:226612258..226612876-chr1:226796174..226796960,2	K562	blood:
15	chr1:226735137..226735678-chr1:226796550..226797189,2	MCF-7	breast:
16	chr1:226789996..226792506-chr1:227056884..227059360,2	MCF-7	breast:
17	chr1:226784528..226786182-chr1:226793038..226795397,2	K562	blood:
18	chr1:226784528..226786182-chr1:226793038..226795397,2	K562	blood:
19	chr1:226781867..226783443-chr1:226785494..226787232,2	K562	blood:
20	chr1:226789700..226792954-chr1:226793236..226797673,6	K562	blood:
21	chr1:226789700..226792954-chr1:226793236..226797673,6	K562	blood:
22	chr1:226735114..226736071-chr1:226796196..226797114,2	MCF-7	breast:
23	chr1:226735519..226736245-chr1:226796429..226797178,4	K562	blood:
24	chr1:226779023..226781177-chr1:226804892..226807313,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSEN2-4	chr1:226793666-226796180	NONHSAT009898
2	lnc-PSEN2-5	chr1:226788290-226788375	NONHSAT009897
3	lnc-PSEN2-5	chr1:226789707-226789895	NONHSAT009897

No data

Variant related genes	Relation type
C1orf95	TF binding region
C1orf95	CpG island
ENSG00000203685	chromatin interactions
ENSG00000143801	chromatin interactions
ENSG00000163050	chromatin interactions

Extended variants
information (count: 1168 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1168 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183960818	chr1:226780029-226780030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373148169	chr1:226780045-226780046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs581400	chr1:226780046-226780047	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs537650659	chr1:226780052-226780053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369944083	chr1:226780101-226780102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556382568	chr1:226780203-226780204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571466811	chr1:226780207-226780208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551435872	chr1:226780260-226780261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs708752	chr1:226780308-226780309	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs553782767	chr1:226780321-226780322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544576200	chr1:226780336-226780337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10799361	chr1:226780346-226780347	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs188738960	chr1:226780358-226780359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554708672	chr1:226780378-226780379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533348647	chr1:226780529-226780530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143190261	chr1:226780548-226780549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544492410	chr1:226780549-226780550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563167241	chr1:226780574-226780575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559570800	chr1:226780580-226780581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545330778	chr1:226780587-226780588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372818127	chr1:226780597-226780598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560107175	chr1:226780609-226780610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180770909	chr1:226780612-226780613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147171367	chr1:226780614-226780615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567664589	chr1:226780624-226780625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531500190	chr1:226780716-226780717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185216947	chr1:226780731-226780732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571449538	chr1:226780758-226780759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10916011	chr1:226780762-226780763	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs374310306	chr1:226780767-226780768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534835454	chr1:226780785-226780786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565632454	chr1:226780814-226780815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566825382	chr1:226780824-226780825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368735723	chr1:226780835-226780836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371185534	chr1:226780836-226780837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569280345	chr1:226780841-226780842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569589374	chr1:226780886-226780887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72490675	chr1:226780887-226780888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs397776250	chr1:226780904-226780905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144206105	chr1:226780925-226780926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188215996	chr1:226780980-226780981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530162458	chr1:226781013-226781014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367657747	chr1:226781026-226781027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182276773	chr1:226781045-226781046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557750152	chr1:226781057-226781058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548682116	chr1:226781103-226781104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187194861	chr1:226781231-226781232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563594756	chr1:226781254-226781255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561406129	chr1:226781255-226781256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs151132788	chr1:226781258-226781259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
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
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
Breast cancer	17603634	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
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:226765000-226790000	Weak transcription	Right Atrium	heart
2	chr1:226774800-226790200	Weak transcription	Fetal Intestine Small	intestine
3	chr1:226776800-226783600	Weak transcription	Stomach Smooth Muscle	stomach
4	chr1:226777400-226783200	Weak transcription	Brain Anterior Caudate	brain
5	chr1:226778800-226790400	Weak transcription	Fetal Brain Female	brain
6	chr1:226781000-226781400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr1:226781400-226781600	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr1:226781800-226782000	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr1:226782000-226784400	Weak transcription	Brain Substantia Nigra	brain
10	chr1:226783200-226783600	ZNF genes & repeats	Brain Anterior Caudate	brain
11	chr1:226783400-226784000	ZNF genes & repeats	Fetal Stomach	stomach
12	chr1:226783600-226784000	Strong transcription	Stomach Smooth Muscle	stomach
13	chr1:226783600-226784200	Weak transcription	Brain Anterior Caudate	brain
14	chr1:226784000-226784600	Weak transcription	Stomach Smooth Muscle	stomach
15	chr1:226784000-226785200	Enhancers	Brain Hippocampus Middle	brain
16	chr1:226784000-226785400	Weak transcription	Fetal Stomach	stomach
17	chr1:226784000-226790200	Weak transcription	Colon Smooth Muscle	Colon
18	chr1:226784200-226784400	Weak transcription	Fetal Muscle Leg	muscle
19	chr1:226784200-226785000	Bivalent Enhancer	HSMMtube	muscle
20	chr1:226784200-226785200	Enhancers	Brain Anterior Caudate	brain
21	chr1:226784400-226784600	Enhancers	Fetal Muscle Leg	muscle
22	chr1:226784400-226784800	Enhancers	Brain Substantia Nigra	brain
23	chr1:226784600-226787600	Weak transcription	Fetal Muscle Leg	muscle
24	chr1:226784800-226790000	Weak transcription	Brain Substantia Nigra	brain
25	chr1:226785200-226790200	Weak transcription	Brain Anterior Caudate	brain
26	chr1:226785400-226785600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr1:226785400-226786200	Enhancers	Fetal Thymus	thymus
28	chr1:226785600-226786400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:226785600-226786400	Enhancers	Placenta Amnion	Placenta Amnion
30	chr1:226785600-226786600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:226785600-226787200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr1:226786000-226786200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:226786000-226789600	Weak transcription	Brain Germinal Matrix	brain
34	chr1:226786200-226786400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr1:226786200-226786400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:226786200-226790000	Weak transcription	Fetal Thymus	thymus
37	chr1:226786400-226786600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr1:226786400-226789600	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr1:226786400-226790000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:226786600-226789200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:226787600-226788400	Enhancers	Fetal Muscle Leg	muscle
42	chr1:226788000-226788200	Enhancers	Fetal Brain Male	brain
43	chr1:226788000-226788200	Bivalent Enhancer	Fetal Stomach	stomach
44	chr1:226788000-226788400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr1:226788200-226788400	Enhancers	Fetal Stomach	stomach
46	chr1:226788200-226789600	Weak transcription	Fetal Brain Male	brain
47	chr1:226788400-226789200	Weak transcription	Fetal Muscle Leg	muscle
48	chr1:226788400-226789600	Weak transcription	Fetal Stomach	stomach
49	chr1:226789200-226789400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr1:226789200-226789800	Enhancers	Fetal Muscle Trunk	muscle

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