Variant report

Variant	esv3334222
Chromosome Location	chr2:73867401-73923991
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	chr2:73907394-73907641	K562	blood:	n/a	n/a
2	ARID3A	chr2:73907372-73907682	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:73869857-73870120	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:73867690-73868035	HepG2	liver:	n/a	n/a
5	ATF2	chr2:73901924-73902346	GM12878	blood:	n/a	n/a
6	ATF3	chr2:73903390-73903706	K562	blood:	n/a	n/a
7	BACH1	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
9	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
10	BATF	chr2:73911582-73911820	GM12878	blood:	n/a	chr2:73911707-73911718
11	BATF	chr2:73917830-73918048	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:73915732-73916019	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
14	BHLHE40	chr2:73917955-73917976	K562	blood:	n/a	n/a
15	BHLHE40	chr2:73871815-73871977	K562	blood:	n/a	n/a
16	CEBPB	chr2:73867603-73868071	MCF-7	breast:	n/a	chr2:73867845-73867858
17	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
18	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
19	CEBPB	chr2:73869472-73869730	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:73867669-73868041	HepG2	liver:	n/a	chr2:73867845-73867858
21	CEBPB	chr2:73867630-73868101	MCF-7	breast:	n/a	chr2:73867845-73867858
22	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
23	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
25	CEBPB	chr2:73869492-73869669	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
27	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
28	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
29	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
30	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
32	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
33	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
34	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
35	CEBPB	chr2:73869936-73870184	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
37	CEBPB	chr2:73867840-73867965	A549	lung:	n/a	chr2:73867845-73867858
38	CHD2	chr2:73869804-73870074	HepG2	liver:	n/a	n/a
39	CTCF	chr2:73907360-73907510	HL-60	blood:	n/a	n/a
40	CTCF	chr2:73917960-73918110	HMF	breast:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
41	CTCF	chr2:73907440-73907590	HA-sp	spinal cord:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
42	CTCF	chr2:73917319-73917375	GM20000	blood:	n/a	n/a
43	CTCF	chr2:73907420-73907570	AG09319	gingival:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
44	CTCF	chr2:73907220-73907370	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr2:73874980-73875130	GM12864	blood:	n/a	n/a
46	CTCF	chr2:73907333-73907669	IMR90	lung:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
47	CTCF	chr2:73907391-73907621	ProgFib	skin:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
48	CTCF	chr2:73912260-73912410	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr2:73907184-73907748	SK-N-SH	brain:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
50	CTCF	chr2:73917940-73918090	GM12865	blood:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73870294-73870344	IMR90	lung:	fetal
2	chr2:73870294-73870344	IMR90	lung:	fetal
3	chr2:73869516-73869566	PFSK-1	brain:	n/a
4	chr2:73907327-73907377	NHBE	bronchial:	n/a
5	chr2:73871855-73871905	AoSMC	blood vessel:	n/a
6	chr2:73871230-73871280	HRCEpiC	kidney:	n/a
7	chr2:73871855-73871905	K562	blood:	n/a
8	chr2:73869516-73869566	HNPCEpiC	eye:	n/a
9	chr2:73871782-73871832	GM12878	blood:	n/a
10	chr2:73870294-73870344	NH-A	brain:	n/a
11	chr2:73869516-73869566	HCM	heart:	n/a
12	chr2:73868736-73868786	IMR90	lung:	fetal
13	chr2:73868919-73868969	HNPCEpiC	eye:	n/a
14	chr2:73869966-73870016	CMK	blood:	n/a
15	chr2:73871855-73871905	U87	brain:	n/a
16	chr2:73871782-73871832	AoSMC	blood vessel:	n/a
17	chr2:73871855-73871905	GM12892	blood:	n/a
18	chr2:73869966-73870016	SK-N-SH_RA	brain:	n/a
19	chr2:73869516-73869566	HMEC	breast:	n/a
20	chr2:73871849-73871899	NH-A	brain:	n/a
21	chr2:73868917-73868967	HIPEpiC	eye:	n/a
22	chr2:73869666-73869716	U87	brain:	n/a
23	chr2:73869516-73869566	U87	brain:	n/a
24	chr2:73871782-73871832	HPAEpiC	pulmonary alveolar:	n/a
25	chr2:73871230-73871280	HCM	heart:	n/a
26	chr2:73871915-73871965	HEEpiC	esophagus:	n/a
27	chr2:73871915-73871965	AG04450	lung:	fetal
28	chr2:73870653-73870703	ovcar-3	ovarian:	n/a
29	chr2:73869666-73869716	HRCEpiC	kidney:	n/a
30	chr2:73870653-73870703	HepG2	liver:	n/a
31	chr2:73868917-73868967	Hela-S3	cervix:	n/a
32	chr2:73871309-73871359	Jurkat	blood:	n/a
33	chr2:73868917-73868967	NB4	blood:	n/a
34	chr2:73870105-73870155	SK-N-SH	brain:	n/a
35	chr2:73869666-73869716	GM12892	blood:	n/a
36	chr2:73871915-73871965	AG04449	skin:	fetal
37	chr2:73871915-73871965	AG09319	gingival:	n/a
38	chr2:73868917-73868967	HCPEpiC	choroid plexus:	n/a
39	chr2:73871230-73871280	Caco-2	colon:	n/a
40	chr2:73871915-73871965	SAEC	small airway:	n/a
41	chr2:73869666-73869716	ECC-1	luminal epithelium:	n/a
42	chr2:73871915-73871965	RPTEC	kidney:	n/a
43	chr2:73871915-73871965	ovcar-3	ovarian:	n/a
44	chr2:73868919-73868969	T-47D	breast:	n/a
45	chr2:73869666-73869716	HMEC	breast:	n/a
46	chr2:73870105-73870155	MCF10A-Er-Src	breast:	n/a
47	chr2:73871915-73871965	AoSMC	blood vessel:	n/a
48	chr2:73871915-73871965	BJ	skin:	n/a
49	chr2:73871230-73871280	GM06990	blood:	n/a
50	chr2:73868736-73868786	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
2	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
3	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
4	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
5	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
6	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
7	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
8	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
9	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
10	chr2:73920861..73923082-chr2:73929614..73932212,2	K562	blood:
11	chr2:73907051..73907568-chr2:74006793..74007607,2	MCF-7	breast:
12	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
13	chr2:73907073..73907951-chr2:74066396..74067279,2	MCF-7	breast:
14	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:
15	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
16	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALMS1-3	chr2:73898207-73898277	NR_003683
2	lnc-ALMS1-3	chr2:73900940-73901123	NR_003683
3	lnc-ALMS1-3	chr2:73899935-73900177	NR_003683
4	lnc-ALMS1-2	chr2:73868076-73868755	NONHSAT071625
5	lnc-ALMS1-3	chr2:73901969-73902032	NR_003683
6	lnc-ALMS1-3	chr2:73912088-73912694	NR_003683
7	lnc-ALMS1-3	chr2:73872046-73872281	NR_003683
8	lnc-ALMS1-3	chr2:73899436-73899622	NR_003683

Variant related genes	Relation type
ALMS1P	TF binding region
NAT8	TF binding region
ALMS1P	CpG island
NAT8	CpG island
ENSG00000144048	chromatin interactions
ENSG00000204872	chromatin interactions

Extended variants
information (count: 2068 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2068 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537017097	chr2:73867401-73867402	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112203138	chr2:73867421-73867422	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577420418	chr2:73867444-73867445	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs386647349	chr2:73867460-73867461	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs67642773	chr2:73867461-73867462	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1879665	chr2:73867469-73867470	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1879664	chr2:73867476-73867477	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
8	rs1879663	chr2:73867494-73867495	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574725277	chr2:73867515-73867516	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541898082	chr2:73867521-73867522	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563411730	chr2:73867570-73867571	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs185515499	chr2:73867596-73867597	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs552501771	chr2:73867602-73867603	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs564324646	chr2:73867618-73867619	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs532431654	chr2:73867619-73867620	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs547411416	chr2:73867652-73867653	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs189277129	chr2:73867667-73867668	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs192278535	chr2:73867678-73867679	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs548422154	chr2:73867694-73867695	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs111302807	chr2:73867700-73867701	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs531694364	chr2:73867757-73867758	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536752161	chr2:73867761-73867762	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs13421413	chr2:73867773-73867774	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs139207855	chr2:73867775-73867776	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs550306777	chr2:73867814-73867815	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs184267281	chr2:73867833-73867834	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs535310791	chr2:73867855-73867856	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs4547554	chr2:73867862-73867863	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs574812822	chr2:73867896-73867897	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs1879662	chr2:73867897-73867898	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs35176564	chr2:73867924-73867925	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs563547940	chr2:73867943-73867944	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs4455178	chr2:73867945-73867946	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs546025211	chr2:73867954-73867955	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs1062881	chr2:73867985-73867986	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs1062880	chr2:73867986-73867987	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs564493980	chr2:73868002-73868003	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs1062879	chr2:73868003-73868004	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs1062878	chr2:73868005-73868006	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs547757802	chr2:73868018-73868019	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs377751721	chr2:73868024-73868025	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs1062877	chr2:73868033-73868034	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs369854513	chr2:73868036-73868037	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs1062876	chr2:73868060-73868061	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs1062875	chr2:73868070-73868071	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs1062874	chr2:73868075-73868076	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs17850955	chr2:73868076-73868077	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs201214893	chr2:73868079-73868080	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs1062873	chr2:73868080-73868081	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs1062872	chr2:73868085-73868086	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73865200-73867600	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr2:73865400-73868000	Weak transcription	Duodenum Mucosa	Duodenum
3	chr2:73865400-73868000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr2:73866200-73870600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:73866400-73868800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr2:73866400-73871200	Enhancers	Fetal Lung	lung
7	chr2:73866600-73867600	Enhancers	HepG2	liver
8	chr2:73866800-73867800	Weak transcription	Spleen	Spleen
9	chr2:73867000-73868200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:73867000-73868600	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr2:73867000-73872200	Enhancers	Ovary	ovary
12	chr2:73867200-73869000	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr2:73867200-73869800	Enhancers	Colonic Mucosa	Colon
14	chr2:73867400-73867800	Weak transcription	Placenta	Placenta
15	chr2:73867400-73868400	Enhancers	Brain Hippocampus Middle	brain
16	chr2:73867400-73868600	Enhancers	Adipose Nuclei	Adipose
17	chr2:73867400-73868600	Enhancers	Brain Cingulate Gyrus	brain
18	chr2:73867400-73869800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr2:73867400-73870200	Flanking Active TSS	Liver	Liver
20	chr2:73867400-73870200	Enhancers	Fetal Intestine Large	intestine
21	chr2:73867600-73867800	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr2:73867600-73868000	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr2:73867600-73868000	Flanking Active TSS	HepG2	liver
24	chr2:73867600-73868200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr2:73867600-73868200	Enhancers	Brain Anterior Caudate	brain
26	chr2:73867600-73868400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr2:73867600-73868400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr2:73867600-73868400	Enhancers	Pancreas	Pancrea
29	chr2:73867600-73868600	Enhancers	Brain Angular Gyrus	brain
30	chr2:73867600-73868600	Enhancers	Brain Substantia Nigra	brain
31	chr2:73867600-73868600	Enhancers	Lung	lung
32	chr2:73867600-73868600	Enhancers	Stomach Mucosa	stomach
33	chr2:73867600-73872200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr2:73867800-73868000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr2:73867800-73868000	Enhancers	HSMMtube	muscle
36	chr2:73867800-73868400	Enhancers	Spleen	Spleen
37	chr2:73867800-73868600	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr2:73867800-73870000	Enhancers	Placenta	Placenta
39	chr2:73868000-73868200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
40	chr2:73868000-73868600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr2:73868000-73868600	Enhancers	Gastric	stomach
42	chr2:73868000-73868800	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr2:73868000-73869000	Flanking Bivalent TSS/Enh	HepG2	liver
44	chr2:73868000-73869200	Enhancers	Duodenum Mucosa	Duodenum
45	chr2:73868200-73868400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr2:73868200-73868400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr2:73868200-73868400	Enhancers	Left Ventricle	heart
48	chr2:73868200-73868600	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr2:73868200-73869800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr2:73868200-73870000	Enhancers	Fetal Intestine Small	intestine

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