Variant report

Variant	esv1802694
Chromosome Location	chr1:226032229-226036309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:486)
CpG islands
(count:244)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:226033582-226033809	HepG2	liver:	n/a	n/a
2	ATF2	chr1:226035614-226036271	GM12878	blood:	n/a	n/a
3	ATF2	chr1:226033441-226033940	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:226033629-226033650	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr1:226033373-226033982	A549	lung:	n/a	n/a
6	BCL3	chr1:226033089-226033715	A549	lung:	n/a	n/a
7	BCLAF1	chr1:226035620-226036437	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:226033488-226033821	K562	blood:	n/a	n/a
9	BHLHE40	chr1:226035781-226036130	GM12878	blood:	n/a	n/a
10	BRCA1	chr1:226033520-226033817	HepG2	liver:	n/a	n/a
11	BRCA1	chr1:226035747-226036097	GM12878	blood:	n/a	n/a
12	BRCA1	chr1:226033564-226033803	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr1:226033446-226033847	K562	blood:	n/a	n/a
14	CEBPB	chr1:226033562-226033800	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:226033576-226033722	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPD	chr1:226033522-226033874	HepG2	liver:	n/a	n/a
17	CHD2	chr1:226035700-226036005	GM12878	blood:	n/a	n/a
18	CHD2	chr1:226033513-226033725	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr1:226033592-226033669	K562	blood:	n/a	n/a
20	CHD2	chr1:226033376-226033616	HepG2	liver:	n/a	n/a
21	CHD2	chr1:226033345-226033855	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr1:226033614-226033745	GM13976	blood:	n/a	n/a
23	CTCF	chr1:226033620-226033770	HAc	cerebellar:	n/a	n/a
24	CTCF	chr1:226033897-226033992	NHEK	skin:	n/a	n/a
25	CTCF	chr1:226033482-226033865	GM12878	blood:	n/a	n/a
26	CTCF	chr1:226033600-226033750	GM12872	blood:	n/a	n/a
27	CTCF	chr1:226033600-226033750	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr1:226033600-226033750	HMF	breast:	n/a	n/a
29	CTCF	chr1:226033600-226033750	BJ	skin:	n/a	n/a
30	CTCF	chr1:226033526-226033816	GM12891	blood:	n/a	n/a
31	CTCF	chr1:226033600-226033750	GM12873	blood:	n/a	n/a
32	CTCF	chr1:226033640-226033790	GM12869	blood:	n/a	n/a
33	CTCF	chr1:226033600-226033750	GM12871	blood:	n/a	n/a
34	CTCF	chr1:226033600-226033750	GM12878	blood:	n/a	n/a
35	CTCF	chr1:226033495-226033827	ECC-1	luminal epithelium:	n/a	n/a
36	CTCF	chr1:226033620-226033770	HepG2	liver:	n/a	n/a
37	CTCF	chr1:226033560-226033710	GM12875	blood:	n/a	n/a
38	CTCF	chr1:226033580-226033730	RPTEC	kidney:	n/a	n/a
39	CTCF	chr1:226033620-226033770	HCT-116	colon:	n/a	n/a
40	CTCF	chr1:226033114-226034481	SK-N-SH	brain:	n/a	n/a
41	CTCF	chr1:226033600-226033750	HFF	foreskin:	n/a	n/a
42	CTCF	chr1:226033580-226033730	HepG2	liver:	n/a	n/a
43	CTCF	chr1:226033620-226033770	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr1:226033620-226033770	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr1:226033580-226033730	GM06990	blood:	n/a	n/a
46	CTCF	chr1:226033580-226033730	GM12875	blood:	n/a	n/a
47	CTCF	chr1:226033640-226033790	GM12801	blood:	n/a	n/a
48	CTCF	chr1:226033560-226033801	Lung_OC	lung:	n/a	n/a
49	CTCF	chr1:226033600-226033750	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr1:226033600-226033750	AG04450	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:226033550-226033600	HCM	heart:	n/a
2	chr1:226033550-226033600	HNPCEpiC	eye:	n/a
3	chr1:226033016-226033066	HRPEpiC	eye:	n/a
4	chr1:226033217-226033267	HL-60	blood:	n/a
5	chr1:226036279-226036329	HNPCEpiC	eye:	n/a
6	chr1:226033016-226033066	Hepatocyte	liver:	n/a
7	chr1:226033016-226033066	MCF10A-Er-Src	breast:	n/a
8	chr1:226033217-226033267	SK-N-MC	brain:	n/a
9	chr1:226036279-226036329	HRCEpiC	kidney:	n/a
10	chr1:226036279-226036329	ProgFib	skin:	n/a
11	chr1:226036279-226036329	Caco-2	colon:	n/a
12	chr1:226036279-226036329	HCPEpiC	choroid plexus:	n/a
13	chr1:226033550-226033600	HCPEpiC	choroid plexus:	n/a
14	chr1:226033550-226033600	HPAEpiC	pulmonary alveolar:	n/a
15	chr1:226033550-226033600	NT2-D1	testis:	n/a
16	chr1:226033016-226033066	AoSMC	blood vessel:	n/a
17	chr1:226033016-226033066	HUVEC	blood vessel:	n/a
18	chr1:226033550-226033600	GM06990	blood:	n/a
19	chr1:226033217-226033267	BJ	skin:	n/a
20	chr1:226033016-226033066	HCT-116	colon:	n/a
21	chr1:226036279-226036329	MCF10A-Er-Src	breast:	n/a
22	chr1:226033550-226033600	HCF	heart:	n/a
23	chr1:226033016-226033066	GM12892	blood:	n/a
24	chr1:226033016-226033066	IMR90	lung:	fetal
25	chr1:226036279-226036329	AG04449	skin:	fetal
26	chr1:226036279-226036329	HepG2	liver:	n/a
27	chr1:226033550-226033600	IMR90	lung:	fetal
28	chr1:226033016-226033066	T-47D	breast:	n/a
29	chr1:226033016-226033066	Caco-2	colon:	n/a
30	chr1:226033550-226033600	HIPEpiC	eye:	n/a
31	chr1:226033217-226033267	AG09309	skin:	n/a
32	chr1:226036279-226036329	T-47D	breast:	n/a
33	chr1:226036279-226036329	K562	blood:	n/a
34	chr1:226033550-226033600	HAEpiC	amniotic membrane:	n/a
35	chr1:226036279-226036329	A549	lung:	n/a
36	chr1:226033016-226033066	A549	lung:	n/a
37	chr1:226033016-226033066	NHDF-neo	bronchial:	n/a
38	chr1:226033550-226033600	SK-N-SH	brain:	n/a
39	chr1:226033217-226033267	NB4	blood:	n/a
40	chr1:226033016-226033066	HCF	heart:	n/a
41	chr1:226033217-226033267	Jurkat	blood:	n/a
42	chr1:226033016-226033066	GM12878	blood:	n/a
43	chr1:226033016-226033066	ECC-1	luminal epithelium:	n/a
44	chr1:226033217-226033267	GM12878	blood:	n/a
45	chr1:226036279-226036329	H1-hESC	embryonic stem cell:	embryo
46	chr1:226033016-226033066	MCF-7	breast:	n/a
47	chr1:226033550-226033600	A549	lung:	n/a
48	chr1:226033016-226033066	K562	blood:	n/a
49	chr1:226033550-226033600	NHDF-neo	bronchial:	n/a
50	chr1:226033550-226033600	LNCaP	prostate:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:226025810..226027984-chr1:226031798..226033532,2	MCF-7	breast:
2	chr1:226034669..226036597-chr1:226045740..226048084,2	K562	blood:
3	chr1:225964257..225969087-chr1:226030786..226035881,7	K562	blood:
4	chr1:225662402..225663343-chr1:226032820..226034152,12	MCF-7	breast:
5	chr1:226033230..226036408-chr1:226061975..226066194,3	MCF-7	breast:
6	chr1:226030085..226032295-chr1:226067898..226070113,2	MCF-7	breast:
7	chr1:226032510..226034899-chr1:226069383..226071490,2	MCF-7	breast:
8	chr1:226033213..226034060-chr1:226163734..226164318,2	K562	blood:
9	chr1:225662312..225663277-chr1:226032721..226034082,11	MCF-7	breast:
10	chr1:226036089..226038052-chr1:226109986..226111681,2	MCF-7	breast:
11	chr1:225963673..225968224-chr1:226032543..226034938,4	MCF-7	breast:
12	chr1:226032890..226033728-chr14:71284226..71284855,2	MCF-7	breast:
13	chr1:226032235..226034217-chr1:226150384..226152008,2	K562	blood:
14	chr1:225964834..225965851-chr1:226033204..226034086,4	K562	blood:
15	chr1:226032252..226033753-chr1:226185534..226188258,2	K562	blood:
16	chr1:225963873..225967033-chr1:226031330..226035962,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM63A-1	chr1:226034181-226034223	ENSG00000242861.1

No data

Variant related genes	Relation type
TMEM63A	TF binding region
ENSG00000242861	TF binding region
TMEM63A	CpG island
ENSG00000242861	CpG island
ENSG00000196187	chromatin interactions
ENSG00000143751	chromatin interactions
ENSG00000143742	chromatin interactions
ENSG00000213032	chromatin interactions
ENSG00000143811	chromatin interactions

Extended variants
information (count: 221 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:221 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1051741	chr1:226032229-226032230	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556212945	chr1:226032230-226032231	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs558420728	chr1:226032274-226032275	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs72549341	chr1:226032279-226032280	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs368469434	chr1:226032286-226032287	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs537463200	chr1:226032293-226032294	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs373599562	chr1:226032305-226032306	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs2137841	chr1:226032319-226032320	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs372126796	chr1:226032320-226032321	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs150700932	chr1:226032322-226032323	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs566570735	chr1:226032323-226032324	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs375479245	chr1:226032330-226032331	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs566051666	chr1:226032340-226032341	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs202060323	chr1:226032341-226032342	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs372006944	chr1:226032354-226032355	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs45519542	chr1:226032358-226032359	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs202009881	chr1:226032366-226032367	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs374759564	chr1:226032372-226032373	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs35190332	chr1:226032378-226032379	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs556390352	chr1:226032396-226032397	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs35800728	chr1:226032397-226032398	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs2137840	chr1:226032438-226032439	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs544781291	chr1:226032462-226032463	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs576076733	chr1:226032475-226032476	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs186604328	chr1:226032524-226032525	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs572990901	chr1:226032527-226032528	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs540678935	chr1:226032528-226032529	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs45467394	chr1:226032529-226032530	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs4149227	chr1:226032530-226032531	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs550711978	chr1:226032540-226032541	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs563156454	chr1:226032541-226032542	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs45477494	chr1:226032592-226032593	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs533718071	chr1:226032607-226032608	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs376435820	chr1:226032636-226032637	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs551997125	chr1:226032656-226032657	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs4149228	chr1:226032677-226032678	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs534133044	chr1:226032698-226032699	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs549036583	chr1:226032699-226032700	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs567266612	chr1:226032766-226032767	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs374316184	chr1:226032770-226032771	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs555766791	chr1:226032787-226032788	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs577513132	chr1:226032794-226032795	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs538587521	chr1:226032795-226032796	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs200590894	chr1:226032802-226032803	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs372085513	chr1:226032807-226032808	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs572155971	chr1:226032808-226032809	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs542476719	chr1:226032809-226032810	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs375375807	chr1:226032810-226032811	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs369727842	chr1:226032827-226032828	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs562175936	chr1:226032829-226032830	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	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
Developmental delay	21147756	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
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:226013600-226052600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:226013800-226037200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:226014000-226032800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr1:226014600-226035600	Weak transcription	Small Intestine	intestine
5	chr1:226014800-226047800	Weak transcription	Psoas Muscle	Psoas
6	chr1:226015400-226032400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr1:226015400-226033200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr1:226015600-226033600	Weak transcription	K562	blood
9	chr1:226016000-226051000	Weak transcription	NH-A	brain
10	chr1:226016400-226033400	Strong transcription	Fetal Intestine Small	intestine
11	chr1:226016800-226033600	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr1:226017400-226049800	Weak transcription	HUVEC	blood vessel
13	chr1:226020400-226033400	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr1:226020600-226042000	Weak transcription	Hela-S3	cervix
15	chr1:226020600-226042400	Weak transcription	HSMM	muscle
16	chr1:226020800-226033400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr1:226020800-226033800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr1:226021000-226033400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:226022200-226033200	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr1:226022200-226033200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:226022800-226033800	Weak transcription	Stomach Mucosa	stomach
22	chr1:226023000-226039600	Weak transcription	NHDF-Ad	bronchial
23	chr1:226023800-226035800	Weak transcription	Fetal Brain Male	brain
24	chr1:226024000-226032800	Strong transcription	Stomach Smooth Muscle	stomach
25	chr1:226024400-226033200	Strong transcription	Fetal Muscle Leg	muscle
26	chr1:226024600-226032600	Strong transcription	Fetal Stomach	stomach
27	chr1:226024600-226032800	Strong transcription	Skeletal Muscle Female	skeletal muscle
28	chr1:226024600-226034000	Weak transcription	Primary hematopoietic stem cells	blood
29	chr1:226025200-226032600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr1:226025200-226033200	Strong transcription	A549	lung
31	chr1:226025200-226033400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr1:226025400-226032600	Strong transcription	Fetal Lung	lung
33	chr1:226025800-226034800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:226025800-226036400	Strong transcription	Lung	lung
35	chr1:226025800-226036400	Strong transcription	Osteobl	bone
36	chr1:226026000-226033200	Strong transcription	Skeletal Muscle Male	skeletal muscle
37	chr1:226026000-226033400	Strong transcription	Duodenum Smooth Muscle	Duodenum
38	chr1:226026000-226034200	Strong transcription	Ovary	ovary
39	chr1:226026200-226035200	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr1:226026800-226061600	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr1:226027000-226033800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr1:226027200-226033600	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr1:226027800-226033200	Weak transcription	Rectal Smooth Muscle	rectum
44	chr1:226028600-226032600	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr1:226028600-226033800	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr1:226029000-226033600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr1:226029000-226033800	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr1:226029400-226033200	Strong transcription	Brain Anterior Caudate	brain
49	chr1:226029600-226033200	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr1:226029600-226033200	Strong transcription	Brain Cingulate Gyrus	brain

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