Variant report

Variant	nsv873770
Chromosome Location	chr2:30952987-30984850
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:190)
CpG islands
(count:183)
Chromatin interactive
region (count:30)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:190 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:30979164-30979271	K562	blood:	n/a	n/a
2	ATF1	chr2:30979033-30979379	K562	blood:	n/a	n/a
3	ATF3	chr2:30978993-30979413	K562	blood:	n/a	n/a
4	BHLHE40	chr2:30979132-30979226	K562	blood:	n/a	n/a
5	CBX3	chr2:30978961-30979339	K562	blood:	n/a	n/a
6	CCNT2	chr2:30978893-30979241	K562	blood:	n/a	n/a
7	CEBPB	chr2:30958272-30958282	HepG2	liver:	n/a	n/a
8	CTCF	chr2:30970100-30970250	HepG2	liver:	n/a	chr2:30970219-30970228
9	CTCF	chr2:30970141-30970319	MCF-7	breast:	n/a	chr2:30970219-30970228
10	CTCF	chr2:30970260-30970410	A549	lung:	n/a	n/a
11	CTCF	chr2:30970120-30970270	SAEC	small airway:	n/a	chr2:30970219-30970228
12	CTCF	chr2:30968500-30968650	Caco-2	colon:	n/a	n/a
13	CTCF	chr2:30983740-30983990	GM12867	blood:	n/a	n/a
14	CTCF	chr2:30982600-30982750	HEK293	kidney:	n/a	chr2:30982700-30982710
15	CTCF	chr2:30968519-30968554	K562	blood:	n/a	n/a
16	CTCF	chr2:30970231-30970245	Lung_OC	lung:	n/a	n/a
17	CTCF	chr2:30983780-30983930	GM12865	blood:	n/a	n/a
18	CTCF	chr2:30970129-30970346	MCF-7	breast:	n/a	chr2:30970219-30970228
19	CTCF	chr2:30981220-30981370	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr2:30970200-30970350	HepG2	liver:	n/a	chr2:30970219-30970228
21	CTCF	chr2:30983780-30983930	GM12864	blood:	n/a	n/a
22	CTCF	chr2:30983740-30984010	GM12872	blood:	n/a	n/a
23	CTCF	chr2:30970118-30970329	Pancreas_OC	pancreas:	n/a	chr2:30970219-30970228
24	CTCF	chr2:30970117-30970329	MCF-7	breast:	n/a	chr2:30970219-30970228
25	CTCF	chr2:30972863-30972967	Lung_OC	lung:	n/a	n/a
26	CTCF	chr2:30968521-30968562	MCF-7	breast:	n/a	n/a
27	CTCF	chr2:30970128-30970308	MCF-7	breast:	n/a	chr2:30970219-30970228
28	CTCF	chr2:30970140-30970290	MCF-7	breast:	n/a	chr2:30970219-30970228
29	CTCF	chr2:30970107-30970344	MCF-7	breast:	n/a	chr2:30970219-30970228
30	CTCF	chr2:30984100-30984250	GM12873	blood:	n/a	n/a
31	CTCF	chr2:30983940-30984090	HepG2	liver:	n/a	n/a
32	CTCF	chr2:30968516-30968520	MCF-7	breast:	n/a	n/a
33	CTCF	chr2:30968516-30968569	LNCaP	prostate:	n/a	n/a
34	CTCF	chr2:30981280-30981430	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr2:30970257-30970291	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr2:30970140-30970290	Caco-2	colon:	n/a	chr2:30970219-30970228
37	CTCF	chr2:30970160-30970310	GM12873	blood:	n/a	chr2:30970219-30970228
38	CTCF	chr2:30970035-30970431	MCF-7	breast:	n/a	chr2:30970219-30970228
39	CTCF	chr2:30970180-30970330	HCT-116	colon:	n/a	chr2:30970219-30970228
40	CUX1	chr2:30979082-30979355	K562	blood:	n/a	n/a
41	ELF1	chr2:30978744-30979569	MCF-7	breast:	n/a	chr2:30979061-30979074 chr2:30979062-30979073 chr2:30979063-30979072
42	ELF1	chr2:30978864-30979268	K562	blood:	n/a	chr2:30979061-30979074 chr2:30979062-30979073 chr2:30979063-30979072
43	ELF1	chr2:30978718-30979501	MCF-7	breast:	n/a	chr2:30979061-30979074 chr2:30979062-30979073 chr2:30979063-30979072
44	EP300	chr2:30980982-30981575	SK-N-SH_RA	brain:	n/a	chr2:30981141-30981155 chr2:30981012-30981026 chr2:30981547-30981563
45	EP300	chr2:30961385-30961720	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr2:30978805-30979265	T-47D	breast:	n/a	chr2:30979219-30979228 chr2:30979063-30979070
47	EP300	chr2:30978840-30979340	SK-N-SH_RA	brain:	n/a	chr2:30979219-30979228 chr2:30979063-30979070
48	EP300	chr2:30978394-30980285	SK-N-SH	brain:	n/a	chr2:30979544-30979558 chr2:30979219-30979228 chr2:30979063-30979070
49	EP300	chr2:30978759-30979291	MCF-7	breast:	n/a	chr2:30979219-30979228 chr2:30979063-30979070
50	EP300	chr2:30956746-30957117	SK-N-SH_RA	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:30967383-30967433	GM19239	blood:	n/a
2	chr2:30967753-30967803	HCPEpiC	choroid plexus:	n/a
3	chr2:30966534-30966584	Hela-S3	cervix:	n/a
4	chr2:30967753-30967803	NH-A	brain:	n/a
5	chr2:30967753-30967803	CMK	blood:	n/a
6	chr2:30966534-30966584	HNPCEpiC	eye:	n/a
7	chr2:30967383-30967433	Caco-2	colon:	n/a
8	chr2:30966534-30966584	SK-N-SH	brain:	n/a
9	chr2:30967753-30967803	ovcar-3	ovarian:	n/a
10	chr2:30966534-30966584	HEK293	kidney:	embryo
11	chr2:30967383-30967433	LNCaP	prostate:	n/a
12	chr2:30967753-30967803	GM12891	blood:	n/a
13	chr2:30967753-30967803	HCT-116	colon:	n/a
14	chr2:30966534-30966584	HL-60	blood:	n/a
15	chr2:30966534-30966584	PrEC	prostate:	n/a
16	chr2:30967753-30967803	GM12878	blood:	n/a
17	chr2:30966534-30966584	NH-A	brain:	n/a
18	chr2:30967753-30967803	NHDF-neo	bronchial:	n/a
19	chr2:30967383-30967433	HCT-116	colon:	n/a
20	chr2:30967753-30967803	AoSMC	blood vessel:	n/a
21	chr2:30967383-30967433	GM12878	blood:	n/a
22	chr2:30967383-30967433	Jurkat	blood:	n/a
23	chr2:30967383-30967433	SK-N-SH	brain:	n/a
24	chr2:30966534-30966584	GM12878	blood:	n/a
25	chr2:30967753-30967803	GM12892	blood:	n/a
26	chr2:30967753-30967803	BJ	skin:	n/a
27	chr2:30967753-30967803	NHBE	bronchial:	n/a
28	chr2:30966534-30966584	LNCaP	prostate:	n/a
29	chr2:30967383-30967433	HNPCEpiC	eye:	n/a
30	chr2:30967383-30967433	H1-hESC	embryonic stem cell:	embryo
31	chr2:30967753-30967803	Caco-2	colon:	n/a
32	chr2:30967753-30967803	HL-60	blood:	n/a
33	chr2:30967383-30967433	AoSMC	blood vessel:	n/a
34	chr2:30967383-30967433	HL-60	blood:	n/a
35	chr2:30966534-30966584	AG04449	skin:	fetal
36	chr2:30967753-30967803	AG10803	skin:	n/a
37	chr2:30966534-30966584	BE2_C	brain:	n/a
38	chr2:30967753-30967803	IMR90	lung:	fetal
39	chr2:30967383-30967433	AG10803	skin:	n/a
40	chr2:30967753-30967803	NB4	blood:	n/a
41	chr2:30966534-30966584	Jurkat	blood:	n/a
42	chr2:30966534-30966584	ProgFib	skin:	n/a
43	chr2:30967383-30967433	Hepatocyte	liver:	n/a
44	chr2:30966534-30966584	MCF-7	breast:	n/a
45	chr2:30966534-30966584	NHDF-neo	bronchial:	n/a
46	chr2:30967753-30967803	MCF-7	breast:	n/a
47	chr2:30966534-30966584	NHBE	bronchial:	n/a
48	chr2:30967753-30967803	HCM	heart:	n/a
49	chr2:30967383-30967433	HCM	heart:	n/a
50	chr2:30966534-30966584	ECC-1	luminal epithelium:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:30962359..30964293-chr2:30967251..30969409,2	MCF-7	breast:
2	chr2:30967775..30969478-chr2:30977702..30980114,2	MCF-7	breast:
3	chr2:30974357..30976391-chr2:30976860..30980887,3	K562	blood:
4	chr2:30971328..30973922-chr2:30977969..30979743,3	MCF-7	breast:
5	chr2:30974357..30976391-chr2:30976860..30980887,3	K562	blood:
6	chr2:30978342..30980549-chr2:31003793..31005445,2	MCF-7	breast:
7	chr2:30952814..30954771-chr2:30956353..30958327,2	MCF-7	breast:
8	chr2:30958598..30960797-chr2:30966634..30970280,3	MCF-7	breast:
9	chr2:30967775..30969478-chr2:30977702..30980114,2	MCF-7	breast:
10	chr2:30974857..30977136-chr2:31030936..31033444,2	MCF-7	breast:
11	chr2:30977562..30982184-chr2:31026694..31034377,7	MCF-7	breast:
12	chr2:30977154..30980117-chr2:31067172..31070017,2	MCF-7	breast:
13	chr2:30961063..30962605-chr2:30966715..30968285,2	K562	blood:
14	chr2:30969086..30972253-chr2:30973250..30976554,4	K562	blood:
15	chr2:30961063..30963636-chr2:30966785..30969337,2	K562	blood:
16	chr2:30974420..30976391-chr2:30977915..30980887,2	K562	blood:
17	chr2:30971328..30973922-chr2:30977969..30979743,3	MCF-7	breast:
18	chr2:30978882..30982474-chr2:30994656..30997998,4	MCF-7	breast:
19	chr2:30983764..30986545-chr2:30993398..30995373,2	K562	blood:
20	chr2:30969086..30972253-chr2:30973250..30976554,4	K562	blood:
21	chr2:30980803..30983163-chr2:30994133..30996203,2	MCF-7	breast:
22	chr2:30960123..30961643-chr2:30966181..30968603,2	MCF-7	breast:
23	chr2:30974420..30976391-chr2:30977915..30980887,2	K562	blood:
24	chr2:30980741..30983020-chr2:30986437..30988713,2	K562	blood:
25	chr2:30952814..30954771-chr2:30956353..30958327,2	MCF-7	breast:
26	chr2:30974995..30977156-chr2:31012471..31013998,2	MCF-7	breast:
27	chr2:30962359..30964293-chr2:30967251..30969409,2	MCF-7	breast:
28	chr2:30961063..30962605-chr2:30966715..30968285,2	K562	blood:
29	chr2:30970154..30970707-chr2:31084669..31085548,2	MCF-7	breast:
30	chr2:30961063..30963636-chr2:30966785..30969337,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GALNT14-1	chr2:30969310-30969567	NONHSAT069919

No data

Variant related genes	Relation type
CAPN13	TF binding region
ENSG00000230118	TF binding region
CAPN13	CpG island
ENSG00000230118	CpG island
ENSG00000230118	chromatin interactions
ENSG00000162949	chromatin interactions

Extended variants
information (count: 1596 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1596 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9679386	chr2:30952987-30952988	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139819306	chr2:30952995-30952996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568191617	chr2:30953009-30953010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537539142	chr2:30953051-30953052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185355546	chr2:30953058-30953059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569128975	chr2:30953074-30953075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557001316	chr2:30953090-30953091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570634987	chr2:30953097-30953098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539403932	chr2:30953098-30953099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552961774	chr2:30953151-30953152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560350468	chr2:30953179-30953180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2609910	chr2:30953215-30953216	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs542208612	chr2:30953222-30953223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555905024	chr2:30953231-30953232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575781830	chr2:30953246-30953247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76228230	chr2:30953268-30953269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563341792	chr2:30953289-30953290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79882499	chr2:30953293-30953294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6711743	chr2:30953300-30953301	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs373108521	chr2:30953349-30953350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114133175	chr2:30953359-30953360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548919698	chr2:30953369-30953370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116346145	chr2:30953386-30953387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144508007	chr2:30953402-30953403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568361564	chr2:30953426-30953427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530590868	chr2:30953468-30953469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190230373	chr2:30953493-30953494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs193254781	chr2:30953503-30953504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567332907	chr2:30953506-30953507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376718952	chr2:30953512-30953513	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570574266	chr2:30953513-30953514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539587295	chr2:30953535-30953536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553331143	chr2:30953545-30953546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566777825	chr2:30953563-30953564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538002071	chr2:30953574-30953575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148437016	chr2:30953585-30953586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531637395	chr2:30953679-30953680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377762647	chr2:30953687-30953688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78952333	chr2:30953762-30953763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575914078	chr2:30953781-30953782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538393830	chr2:30953796-30953797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184857435	chr2:30953822-30953823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577001444	chr2:30953842-30953843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545966663	chr2:30953855-30953856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188105865	chr2:30953892-30953893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs180967829	chr2:30953925-30953926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541831262	chr2:30953951-30953952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561787445	chr2:30954003-30954004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531743072	chr2:30954006-30954007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6756860	chr2:30954016-30954017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Medulloblastoma	16968546	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	18927303	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:30902400-30954000	Weak transcription	Gastric	stomach
2	chr2:30940600-30969600	Weak transcription	Stomach Mucosa	stomach
3	chr2:30945800-30955400	Weak transcription	Fetal Intestine Small	intestine
4	chr2:30946800-30953200	Weak transcription	Fetal Stomach	stomach
5	chr2:30947400-30953000	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr2:30950000-30954200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr2:30951400-30954000	Strong transcription	Rectal Mucosa Donor 31	rectum
8	chr2:30953000-30953600	Strong transcription	Rectal Mucosa Donor 29	rectum
9	chr2:30953200-30954000	Strong transcription	Fetal Stomach	stomach
10	chr2:30953600-30965200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr2:30954000-30955800	Strong transcription	Gastric	stomach
12	chr2:30954000-30965400	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr2:30955200-30955400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr2:30955400-30957200	Enhancers	Fetal Intestine Small	intestine
15	chr2:30955400-30959400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr2:30955800-30956000	ZNF genes & repeats	Gastric	stomach
17	chr2:30956000-30964000	Weak transcription	Gastric	stomach
18	chr2:30956400-30957000	Enhancers	Fetal Intestine Large	intestine
19	chr2:30957000-30969800	Weak transcription	Fetal Intestine Large	intestine
20	chr2:30957200-30964400	Weak transcription	Fetal Intestine Small	intestine
21	chr2:30959000-30960000	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr2:30959200-30959800	Enhancers	HMEC	breast
23	chr2:30959400-30959800	Enhancers	NHEK	skin
24	chr2:30959400-30960000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:30959400-30960200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr2:30959400-30960400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr2:30959400-30960600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr2:30959400-30962000	Weak transcription	Right Atrium	heart
29	chr2:30959600-30959800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr2:30960000-30963800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr2:30960200-30960400	Enhancers	Brain Hippocampus Middle	brain
32	chr2:30960400-30980000	Weak transcription	Brain Hippocampus Middle	brain
33	chr2:30961000-30965400	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr2:30961400-30961600	Enhancers	Pancreas	Pancrea
35	chr2:30961400-30964800	Weak transcription	Fetal Stomach	stomach
36	chr2:30961600-30978400	Weak transcription	Pancreas	Pancrea
37	chr2:30962000-30970200	Weak transcription	Brain Substantia Nigra	brain
38	chr2:30962600-30967600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:30963600-30969600	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr2:30963800-30964800	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr2:30964000-30964400	Enhancers	Adipose Nuclei	Adipose
42	chr2:30964000-30970600	Strong transcription	Gastric	stomach
43	chr2:30964400-30965400	Weak transcription	Duodenum Mucosa	Duodenum
44	chr2:30964400-30969000	Strong transcription	Fetal Intestine Small	intestine
45	chr2:30964400-30978600	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr2:30964800-30965200	Strong transcription	Fetal Stomach	stomach
47	chr2:30965200-30965600	ZNF genes & repeats	Fetal Stomach	stomach
48	chr2:30965200-30966000	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr2:30965400-30965800	Strong transcription	Pancreatic Islets	Pancreatic Islet
50	chr2:30965400-30966000	Strong transcription	Duodenum Mucosa	Duodenum

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