Variant report

Variant	nsv874889
Chromosome Location	chr2:113796666-113814670
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	BCLAF1	chr2:113808322-113808787	K562	blood:	n/a	n/a
2	BCLAF1	chr2:113808248-113808885	K562	blood:	n/a	n/a
3	CBX3	chr2:113812744-113813121	K562	blood:	n/a	n/a
4	CBX3	chr2:113812793-113813116	K562	blood:	n/a	n/a
5	CBX3	chr2:113808363-113808794	K562	blood:	n/a	n/a
6	CBX3	chr2:113808267-113808819	K562	blood:	n/a	n/a
7	CCNT2	chr2:113808487-113808687	K562	blood:	n/a	n/a
8	CEBPB	chr2:113813626-113813695	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:113813636-113813677	IMR90	lung:	n/a	n/a
10	CHD2	chr2:113808657-113808709	K562	blood:	n/a	n/a
11	CTCF	chr2:113799620-113799770	GM12867	blood:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
12	CTCF	chr2:113799540-113799690	GM12864	blood:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
13	CTCF	chr2:113799580-113799730	SAEC	small airway:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
14	CTCF	chr2:113808568-113808720	GM19239	blood:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808675-113808696 chr2:113808682-113808695
15	CTCF	chr2:113799600-113799750	Caco-2	colon:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
16	CTCF	chr2:113799540-113799690	GM12865	blood:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
17	CTCF	chr2:113808680-113808830	HCM	heart:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808682-113808695
18	CTCF	chr2:113808640-113808790	MCF-7	breast:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808675-113808696 chr2:113808682-113808695
19	CTCF	chr2:113799493-113799811	K562	blood:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
20	CTCF	chr2:113799620-113799770	GM06990	blood:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
21	CTCF	chr2:113799478-113799792	H1-hESC	embryonic stem cell:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
22	CTCF	chr2:113799536-113799766	K562	blood:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
23	CTCF	chr2:113799397-113799872	HCT-116	colon:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
24	CTCF	chr2:113799558-113799760	MCF-7	breast:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
25	CTCF	chr2:113799645-113799674	GM13977	blood:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
26	CTCF	chr2:113808549-113808763	HepG2	liver:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808675-113808696 chr2:113808682-113808695
27	CTCF	chr2:113799540-113799690	HBMEC	blood vessel:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
28	CTCF	chr2:113808527-113808836	K562	blood:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808675-113808696 chr2:113808682-113808695
29	CTCF	chr2:113808612-113808729	A549	lung:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808675-113808696 chr2:113808682-113808695
30	CTCF	chr2:113799500-113799650	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr2:113799560-113799710	RPTEC	kidney:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
32	CTCF	chr2:113808680-113808830	HBMEC	blood vessel:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808682-113808695
33	CTCF	chr2:113799680-113799830	HFF	foreskin:	n/a	n/a
34	CTCF	chr2:113799551-113799739	GM12892	blood:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
35	CTCF	chr2:113799418-113799912	MCF-7	breast:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
36	CTCF	chr2:113799580-113799730	GM12869	blood:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
37	CTCF	chr2:113799480-113799630	GM12866	blood:	n/a	n/a
38	CTCF	chr2:113808640-113808790	HepG2	liver:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808675-113808696 chr2:113808682-113808695
39	CTCF	chr2:113799560-113799710	GM12875	blood:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
40	CTCF	chr2:113808640-113808790	HEK293	kidney:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808675-113808696 chr2:113808682-113808695
41	CTCF	chr2:113799500-113799650	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr2:113808420-113808570	A549	lung:	n/a	n/a
43	CTCF	chr2:113799600-113799750	MCF-7	breast:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
44	CTCF	chr2:113808694-113808734	Gliobla	brain:	n/a	n/a
45	CTCF	chr2:113799540-113799690	GM12878	blood:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
46	CTCF	chr2:113808615-113808736	GM19240	blood:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808675-113808696 chr2:113808682-113808695
47	CTCF	chr2:113808660-113808810	GM12865	blood:	n/a	chr2:113808681-113808697 chr2:113808680-113808698 chr2:113808682-113808695 chr2:113808675-113808696 chr2:113808682-113808695
48	CTCF	chr2:113808700-113808850	A549	lung:	n/a	n/a
49	CTCF	chr2:113799637-113799672	Pancreas_OC	pancreas:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662
50	CTCF	chr2:113799550-113799739	HepG2	liver:	n/a	chr2:113799648-113799669 chr2:113799647-113799663 chr2:113799646-113799664 chr2:113799649-113799662

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:113808530-113808580	HNPCEpiC	eye:	n/a
2	chr2:113804820-113804870	IMR90	lung:	fetal
3	chr2:113808755-113808805	CMK	blood:	n/a
4	chr2:113808755-113808805	BJ	skin:	n/a
5	chr2:113810244-113810294	Jurkat	blood:	n/a
6	chr2:113808755-113808805	ovcar-3	ovarian:	n/a
7	chr2:113808755-113808805	PFSK-1	brain:	n/a
8	chr2:113810743-113810793	IMR90	lung:	fetal
9	chr2:113808452-113808502	AG04449	skin:	fetal
10	chr2:113810244-113810294	PrEC	prostate:	n/a
11	chr2:113808452-113808502	GM12891	blood:	n/a
12	chr2:113810743-113810793	BE2_C	brain:	n/a
13	chr2:113811250-113811300	PANC-1	pancreas:	n/a
14	chr2:113808452-113808502	Jurkat	blood:	n/a
15	chr2:113810244-113810294	AoSMC	blood vessel:	n/a
16	chr2:113810743-113810793	HMEC	breast:	n/a
17	chr2:113808683-113808733	IMR90	lung:	fetal
18	chr2:113810743-113810793	HIPEpiC	eye:	n/a
19	chr2:113810244-113810294	HEEpiC	esophagus:	n/a
20	chr2:113810244-113810294	Hela-S3	cervix:	n/a
21	chr2:113810743-113810793	GM19239	blood:	n/a
22	chr2:113811250-113811300	NB4	blood:	n/a
23	chr2:113811250-113811300	PrEC	prostate:	n/a
24	chr2:113804820-113804870	ovcar-3	ovarian:	n/a
25	chr2:113808683-113808733	HEEpiC	esophagus:	n/a
26	chr2:113810244-113810294	CMK	blood:	n/a
27	chr2:113808452-113808502	PFSK-1	brain:	n/a
28	chr2:113810641-113810691	GM12891	blood:	n/a
29	chr2:113808530-113808580	HEEpiC	esophagus:	n/a
30	chr2:113810244-113810294	HPAEpiC	pulmonary alveolar:	n/a
31	chr2:113810244-113810294	ProgFib	skin:	n/a
32	chr2:113810641-113810691	HAEpiC	amniotic membrane:	n/a
33	chr2:113808755-113808805	RPTEC	kidney:	n/a
34	chr2:113808452-113808502	NHDF-neo	bronchial:	n/a
35	chr2:113808683-113808733	Jurkat	blood:	n/a
36	chr2:113810244-113810294	GM12878	blood:	n/a
37	chr2:113810743-113810793	PFSK-1	brain:	n/a
38	chr2:113810743-113810793	HEEpiC	esophagus:	n/a
39	chr2:113808683-113808733	SK-N-SH_RA	brain:	n/a
40	chr2:113808683-113808733	MCF-7	breast:	n/a
41	chr2:113808683-113808733	SK-N-SH	brain:	n/a
42	chr2:113808683-113808733	HepG2	liver:	n/a
43	chr2:113810244-113810294	AG09319	gingival:	n/a
44	chr2:113808452-113808502	BE2_C	brain:	n/a
45	chr2:113810641-113810691	BJ	skin:	n/a
46	chr2:113808755-113808805	HCM	heart:	n/a
47	chr2:113808755-113808805	NH-A	brain:	n/a
48	chr2:113808755-113808805	HepG2	liver:	n/a
49	chr2:113808530-113808580	Hepatocyte	liver:	n/a
50	chr2:113808452-113808502	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:113799300..113800125-chr2:113836934..113837726,3	MCF-7	breast:
2	chr2:113798210..113800371-chr2:113830392..113832016,2	MCF-7	breast:
3	chr2:113808473..113809153-chr2:113816777..113817326,2	K562	blood:
4	chr2:113809110..113811211-chr2:113812737..113815572,2	K562	blood:
5	chr2:113793052..113795828-chr2:113797640..113799974,2	K562	blood:
6	chr2:113793052..113795716-chr2:113797814..113799974,2	K562	blood:
7	chr2:113756681..113759563-chr2:113795115..113796939,2	K562	blood:
8	chr2:113808741..113811211-chr2:113813910..113818157,4	K562	blood:
9	chr2:113808741..113811211-chr2:113813910..113818157,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL36RN-2	chr2:113799365-113799600	l_1927_chr2:113799151-113802812_thyroid
2	lnc-IL36RN-2	chr2:113799152-113799363	l_1927_chr2:113799151-113802812_thyroid
3	lnc-IL36RN-2	chr2:113802726-113802812	l_1927_chr2:113799151-113802812_thyroid

Variant related genes	Relation type
IL36RN	TF binding region
IL36B	TF binding region
IL36RN	CpG island
IL36B	CpG island
ENSG00000136695	chromatin interactions
ENSG00000136696	chromatin interactions

Extended variants
information (count: 570 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1374280	chr2:113796666-113796667	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs113819754	chr2:113796673-113796674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573595269	chr2:113796697-113796698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79613977	chr2:113796698-113796699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556306562	chr2:113796704-113796705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76075666	chr2:113796707-113796708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143757145	chr2:113796740-113796741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564778732	chr2:113796778-113796779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188123999	chr2:113796801-113796802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541020857	chr2:113796837-113796838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561616229	chr2:113796840-113796841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376899039	chr2:113796855-113796856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547177788	chr2:113796950-113796951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530398068	chr2:113796954-113796955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554811096	chr2:113796987-113796988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191805528	chr2:113797113-113797114	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570248337	chr2:113797124-113797125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143176485	chr2:113797142-113797143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533309491	chr2:113797150-113797151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552644362	chr2:113797157-113797158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565825700	chr2:113797172-113797173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534742889	chr2:113797193-113797194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549828034	chr2:113797242-113797243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1446508	chr2:113797261-113797262	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs184347153	chr2:113797267-113797268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535087647	chr2:113797284-113797285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189249733	chr2:113797315-113797316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536561174	chr2:113797362-113797363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556154094	chr2:113797384-113797385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148263369	chr2:113797423-113797424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2862773	chr2:113797444-113797445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372807927	chr2:113797445-113797446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74997617	chr2:113797446-113797447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34015028	chr2:113797447-113797448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs3049662	chr2:113797449-113797450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558662007	chr2:113797464-113797465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572171644	chr2:113797492-113797493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541057455	chr2:113797537-113797538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1900287	chr2:113797565-113797566	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs529680630	chr2:113797595-113797596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112788078	chr2:113797631-113797632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1900288	chr2:113797645-113797646	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs2862774	chr2:113797677-113797678	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs150761350	chr2:113797712-113797713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77516439	chr2:113797741-113797742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528548602	chr2:113797761-113797762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2862775	chr2:113797762-113797763	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs13392105	chr2:113797766-113797767	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs549026167	chr2:113797779-113797780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556428559	chr2:113797819-113797820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
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
Autism	17483303	CNVD
Autism	22495311	CNVD
Autism	18522746	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113765600-113797400	Weak transcription	Gastric	stomach
2	chr2:113795800-113797800	Enhancers	Stomach Mucosa	stomach
3	chr2:113796200-113797600	Enhancers	Pancreas	Pancrea
4	chr2:113796400-113796800	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr2:113796400-113798000	Enhancers	Liver	Liver
6	chr2:113796600-113796800	Enhancers	Fetal Intestine Small	intestine
7	chr2:113796600-113798000	Enhancers	Fetal Intestine Large	intestine
8	chr2:113796800-113797200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr2:113796800-113797400	Enhancers	HepG2	liver
10	chr2:113796800-113797600	Enhancers	Fetal Lung	lung
11	chr2:113797400-113797600	Enhancers	Gastric	stomach
12	chr2:113797600-113797800	Enhancers	Fetal Intestine Small	intestine
13	chr2:113797600-113798600	Weak transcription	Gastric	stomach
14	chr2:113797800-113799800	Weak transcription	Stomach Mucosa	stomach
15	chr2:113798600-113798800	Enhancers	Gastric	stomach
16	chr2:113804600-113805400	Enhancers	Fetal Intestine Large	intestine
17	chr2:113804600-113805400	Enhancers	Fetal Intestine Small	intestine
18	chr2:113805400-113805600	Weak transcription	Fetal Intestine Small	intestine
19	chr2:113805400-113805800	Weak transcription	Fetal Intestine Large	intestine
20	chr2:113805600-113806000	Enhancers	Fetal Intestine Small	intestine
21	chr2:113805800-113806000	Enhancers	Fetal Intestine Large	intestine
22	chr2:113806000-113808600	Weak transcription	Fetal Intestine Large	intestine
23	chr2:113806000-113809000	Weak transcription	Fetal Intestine Small	intestine
24	chr2:113808400-113808800	Weak transcription	Right Atrium	heart
25	chr2:113808600-113811600	Enhancers	Fetal Intestine Large	intestine
26	chr2:113809000-113809200	Enhancers	Fetal Intestine Small	intestine
27	chr2:113809000-113809200	ZNF genes & repeats	Right Atrium	heart
28	chr2:113809200-113809600	Weak transcription	Fetal Intestine Small	intestine
29	chr2:113809400-113813800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr2:113809600-113811200	Enhancers	Fetal Intestine Small	intestine
31	chr2:113811200-113814400	ZNF genes & repeats	Fetal Intestine Small	intestine
32	chr2:113812400-113812600	Bivalent/Poised TSS	Sigmoid Colon	Sigmoid Colon
33	chr2:113812400-113812800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr2:113812600-113812800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr2:113813800-113814200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr2:113813800-113815200	Enhancers	Fetal Intestine Large	intestine
37	chr2:113814200-113816200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr2:113814400-113815000	Weak transcription	Fetal Intestine Small	intestine
39	chr2:113814600-113818400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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