Variant report

Variant	esv2759806
Chromosome Location	chr11:18818729-19082068
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1576)
CpG islands
(count:1039)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1576 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:18824240-18824543	K562	blood:	n/a	chr11:18824427-18824443
2	ARID3A	chr11:18866399-18866660	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:18824216-18824538	HepG2	liver:	n/a	chr11:18824427-18824443
4	ARID3A	chr11:18866389-18866666	K562	blood:	n/a	n/a
5	ATF1	chr11:18824189-18824548	K562	blood:	n/a	n/a
6	ATF1	chr11:18866365-18866566	K562	blood:	n/a	n/a
7	ATF1	chr11:18985505-18985506	K562	blood:	n/a	n/a
8	ATF2	chr11:18824136-18824587	GM12878	blood:	n/a	chr11:18824418-18824425
9	ATF2	chr11:18824169-18824586	GM12878	blood:	n/a	chr11:18824418-18824425
10	ATF2	chr11:18874832-18875250	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr11:18824115-18824599	H1-hESC	embryonic stem cell:	n/a	chr11:18824418-18824425
12	ATF2	chr11:18824092-18824659	H1-hESC	embryonic stem cell:	n/a	chr11:18824418-18824425
13	ATF3	chr11:18824258-18824530	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr11:18824216-18824507	K562	blood:	n/a	n/a
15	ATF3	chr11:18824089-18824453	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr11:18887554-18887781	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL3	chr11:19009442-19009799	GM12878	blood:	n/a	chr11:19009475-19009484
18	BCL3	chr11:19048430-19048840	GM12878	blood:	n/a	n/a
19	BCL3	chr11:19048430-19048742	GM12878	blood:	n/a	n/a
20	BCL3	chr11:19009395-19009756	GM12878	blood:	n/a	chr11:19009475-19009484
21	BHLHE40	chr11:18866437-18866544	GM12878	blood:	n/a	n/a
22	BRCA1	chr11:18836401-18836475	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr11:18827681-18827698	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr11:19009295-19009856	HCT-116	colon:	n/a	n/a
25	CBX3	chr11:19049746-19050118	HCT-116	colon:	n/a	n/a
26	CEBPB	chr11:18824223-18824611	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr11:18824183-18824591	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr11:19075503-19075812	HepG2	liver:	n/a	chr11:19075655-19075666
29	CEBPB	chr11:18886146-18886431	A549	lung:	n/a	chr11:18886280-18886291
30	CEBPB	chr11:19075539-19075817	IMR90	lung:	n/a	chr11:19075655-19075666
31	CEBPB	chr11:19005030-19005105	HepG2	liver:	n/a	chr11:19005074-19005085
32	CEBPB	chr11:18824169-18824629	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr11:18943007-18943263	K562	blood:	n/a	n/a
34	CEBPB	chr11:18824180-18824625	MCF-7	breast:	n/a	n/a
35	CEBPB	chr11:19070943-19071260	A549	lung:	n/a	chr11:19071079-19071090
36	CEBPB	chr11:18824250-18824457	HepG2	liver:	n/a	n/a
37	CEBPB	chr11:19075511-19075778	K562	blood:	n/a	chr11:19075655-19075666
38	CEBPB	chr11:18883959-18884233	IMR90	lung:	n/a	chr11:18884110-18884121
39	CEBPB	chr11:18826088-18826344	HepG2	liver:	n/a	n/a
40	CEBPB	chr11:19070915-19071272	IMR90	lung:	n/a	chr11:19071079-19071090
41	CEBPB	chr11:18946494-18946596	HepG2	liver:	n/a	chr11:18946576-18946587
42	CEBPB	chr11:19049458-19049658	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr11:19070928-19071245	K562	blood:	n/a	chr11:19071079-19071090
44	CEBPB	chr11:19075550-19075793	A549	lung:	n/a	chr11:19075655-19075666
45	CEBPB	chr11:19070121-19070197	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr11:18824120-18824623	MCF-7	breast:	n/a	n/a
47	CEBPB	chr11:18860179-18860379	HepG2	liver:	n/a	chr11:18860276-18860287
48	CEBPB	chr11:18824196-18824581	HepG2	liver:	n/a	n/a
49	CEBPB	chr11:18824179-18824594	IMR90	lung:	n/a	n/a
50	CEBPB	chr11:18886185-18886385	HepG2	liver:	n/a	chr11:18886280-18886291

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18956196-18956246	HCF	heart:	n/a
2	chr11:18956196-18956246	ECC-1	luminal epithelium:	n/a
3	chr11:18956196-18956246	HCF	heart:	n/a
4	chr11:18956196-18956246	ECC-1	luminal epithelium:	n/a
5	chr11:18956196-18956246	HUVEC	blood vessel:	n/a
6	chr11:18978157-18978207	HNPCEpiC	eye:	n/a
7	chr11:18993891-18993941	H1-hESC	embryonic stem cell:	embryo
8	chr11:18993880-18993930	MCF10A-Er-Src	breast:	n/a
9	chr11:18993455-18993505	NH-A	brain:	n/a
10	chr11:18978157-18978207	AG09319	gingival:	n/a
11	chr11:18978218-18978268	SK-N-MC	brain:	n/a
12	chr11:18978169-18978219	HCM	heart:	n/a
13	chr11:19081590-19081640	HPAEpiC	pulmonary alveolar:	n/a
14	chr11:18955977-18956027	NHBE	bronchial:	n/a
15	chr11:18956283-18956333	HCT-116	colon:	n/a
16	chr11:18994080-18994130	SAEC	small airway:	n/a
17	chr11:18887821-18887871	ovcar-3	ovarian:	n/a
18	chr11:18957755-18957805	SAEC	small airway:	n/a
19	chr11:19078052-19078102	PFSK-1	brain:	n/a
20	chr11:18955977-18956027	ovcar-3	ovarian:	n/a
21	chr11:19077763-19077813	HRCEpiC	kidney:	n/a
22	chr11:18978391-18978441	K562	blood:	n/a
23	chr11:18957755-18957805	AG04450	lung:	fetal
24	chr11:18978218-18978268	HNPCEpiC	eye:	n/a
25	chr11:18978391-18978441	NB4	blood:	n/a
26	chr11:19077763-19077813	AG04449	skin:	fetal
27	chr11:18887821-18887871	NB4	blood:	n/a
28	chr11:18978157-18978207	RPTEC	kidney:	n/a
29	chr11:18955977-18956027	SK-N-MC	brain:	n/a
30	chr11:18955977-18956027	Jurkat	blood:	n/a
31	chr11:19078052-19078102	A549	lung:	n/a
32	chr11:18978169-18978219	PANC-1	pancreas:	n/a
33	chr11:19078052-19078102	SK-N-SH	brain:	n/a
34	chr11:18994080-18994130	SK-N-MC	brain:	n/a
35	chr11:18956637-18956687	GM12891	blood:	n/a
36	chr11:19081590-19081640	GM12892	blood:	n/a
37	chr11:18994080-18994130	NHBE	bronchial:	n/a
38	chr11:18994080-18994130	GM06990	blood:	n/a
39	chr11:18956196-18956246	PFSK-1	brain:	n/a
40	chr11:18993455-18993505	HCM	heart:	n/a
41	chr11:19077763-19077813	GM19239	blood:	n/a
42	chr11:18956283-18956333	HRCEpiC	kidney:	n/a
43	chr11:19081590-19081640	NHDF-neo	bronchial:	n/a
44	chr11:18955977-18956027	HMEC	breast:	n/a
45	chr11:18978157-18978207	MCF-7	breast:	n/a
46	chr11:18978169-18978219	RPTEC	kidney:	n/a
47	chr11:19077763-19077813	HIPEpiC	eye:	n/a
48	chr11:18955977-18956027	HepG2	liver:	n/a
49	chr11:18956196-18956246	CMK	blood:	n/a
50	chr11:18993880-18993930	LNCaP	prostate:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:18796976..18797942-chr11:18874533..18875361,2	MCF-7	breast:
2	chr11:18898429..18900473-chr11:18904147..18906021,2	K562	blood:
3	chr11:19040852..19043849-chr11:19051453..19053254,2	K562	blood:
4	chr11:18826995..18828536-chr11:18830032..18832999,2	K562	blood:
5	chr11:18821196..18822809-chr11:18824205..18826880,2	K562	blood:
6	chr11:18866095..18866981-chr11:18874883..18875523,3	MCF-7	breast:
7	chr11:18826995..18828536-chr11:18830032..18832999,2	K562	blood:
8	chr11:19081397..19083267-chr11:19138143..19140482,2	MCF-7	breast:
9	chr11:18869521..18872486-chr11:18872748..18874682,2	MCF-7	breast:
10	chr11:18993520..18994020-chr11:48120012..48120966,2	MCF-7	breast:
11	chr11:18951880..18953861-chr11:18956190..18958282,2	K562	blood:
12	chr11:18797328..18797891-chr11:18823891..18824854,4	MCF-7	breast:
13	chr11:18796941..18797965-chr11:18823862..18824878,5	K562	blood:
14	chr11:18748906..18749558-chr11:18823928..18824847,2	K562	blood:
15	chr11:18898429..18900473-chr11:18904147..18906021,2	K562	blood:
16	chr11:18796828..18797871-chr11:18823982..18825133,8	MCF-7	breast:
17	chr11:18866095..18866981-chr11:18874883..18875523,3	MCF-7	breast:
18	chr11:18948757..18949726-chr11:19092570..19093333,3	MCF-7	breast:
19	chr11:18869521..18872486-chr11:18872748..18874682,2	MCF-7	breast:
20	chr11:18799470..18800368-chr11:18874998..18875508,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRGPRX2-1	chr11:19051244-19051985	NONHSAT018325
2	lnc-MRGPRX1-1	chr11:18885105-18886056	NONHSAT018323
3	lnc-ZDHHC13-2	chr11:18960852-18961268	ENSG00000255244.1
4	lnc-ZDHHC13-2	chr11:18956532-18956821	ENSG00000255244.1

No data

Variant related genes	Relation type
ENSG00000255536	TF binding region
ENSG00000254541	TF binding region
MRGPRX1	TF binding region
ENSG00000254738	TF binding region
ENSG00000255424	TF binding region
ENSG00000265940	TF binding region
ENSG00000255244	TF binding region
ENSG00000254720	TF binding region
ENSG00000255511	TF binding region
PTPN5	TF binding region
ENSG00000254529	TF binding region
ENSG00000255536	CpG island
ENSG00000254541	CpG island
MRGPRX1	CpG island
ENSG00000254738	CpG island
ENSG00000255424	CpG island
ENSG00000265940	CpG island
ENSG00000255244	CpG island
ENSG00000254720	CpG island
ENSG00000255511	CpG island
PTPN5	CpG island
ENSG00000254529	CpG island
ENSG00000255424	chromatin interactions
ENSG00000177054	chromatin interactions
ENSG00000255244	chromatin interactions
ENSG00000170255	chromatin interactions
ENSG00000265940	chromatin interactions

Extended variants
information (count: 5227 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:5227 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535491168	chr11:18818766-18818767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs190812155	chr11:18818784-18818785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537621308	chr11:18818807-18818808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181084219	chr11:18818809-18818810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147172863	chr11:18818828-18818829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185687562	chr11:18818917-18818918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140354779	chr11:18818989-18818990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149669481	chr11:18819015-18819016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553805628	chr11:18819032-18819033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71313421	chr11:18819033-18819034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539554892	chr11:18819034-18819035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs199520636	chr11:18819049-18819050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs398040248	chr11:18819051-18819052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190404586	chr11:18819058-18819059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559268105	chr11:18819199-18819200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113211668	chr11:18819236-18819237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144464487	chr11:18819253-18819254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563051615	chr11:18819281-18819282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571907442	chr11:18819311-18819312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148402252	chr11:18819341-18819342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142720517	chr11:18819360-18819361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182957931	chr11:18819365-18819366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs116554728	chr11:18819376-18819377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375594193	chr11:18819390-18819391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527635804	chr11:18819477-18819478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372564102	chr11:18819541-18819542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552310004	chr11:18819553-18819554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187595356	chr11:18819599-18819600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192154042	chr11:18819673-18819674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549689799	chr11:18819675-18819676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567908786	chr11:18819718-18819719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183929425	chr11:18819731-18819732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146512888	chr11:18819740-18819741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542268688	chr11:18819758-18819759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553786397	chr11:18819773-18819774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557543744	chr11:18819824-18819825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565662076	chr11:18819848-18819849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539387810	chr11:18819907-18819908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557771487	chr11:18819928-18819929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187696173	chr11:18819962-18819963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192317024	chr11:18819970-18819971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs4378359	chr11:18819971-18819972	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs556937047	chr11:18819996-18819997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555943532	chr11:18820021-18820022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574935638	chr11:18820040-18820041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369526058	chr11:18820095-18820096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7123663	chr11:18820109-18820110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144042744	chr11:18820136-18820137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560606061	chr11:18820141-18820142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576215470	chr11:18820167-18820168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ollier disease	21235737	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18818600-18819400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr11:18819400-18822800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr11:18820200-18821000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:18820200-18821000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr11:18820200-18821200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr11:18820200-18821200	Enhancers	HMEC	breast
7	chr11:18820400-18820600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:18820400-18820800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:18820400-18820800	Enhancers	NHEK	skin
10	chr11:18820800-18822600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:18822600-18824400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:18822600-18824600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:18822800-18824200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr11:18823000-18823400	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr11:18823200-18824000	Enhancers	Brain Hippocampus Middle	brain
16	chr11:18823200-18824400	Enhancers	Brain Substantia Nigra	brain
17	chr11:18823400-18823800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr11:18823800-18824000	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr11:18823800-18824000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr11:18823800-18824200	Enhancers	Brain Cingulate Gyrus	brain
21	chr11:18823800-18824400	Enhancers	Brain Anterior Caudate	brain
22	chr11:18824000-18824200	Flanking Active TSS	Brain Hippocampus Middle	brain
23	chr11:18824000-18824200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
24	chr11:18824000-18824200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr11:18824000-18824800	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr11:18824200-18824400	Enhancers	Brain Hippocampus Middle	brain
27	chr11:18824200-18824400	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr11:18824200-18824600	Active TSS	Brain Cingulate Gyrus	brain
29	chr11:18824200-18824600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr11:18824400-18824600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr11:18824400-18824600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr11:18824400-18824600	Flanking Active TSS	Liver	Liver
33	chr11:18824400-18824600	Flanking Active TSS	Brain Anterior Caudate	brain
34	chr11:18824400-18824600	Flanking Active TSS	Brain Hippocampus Middle	brain
35	chr11:18824400-18824600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
36	chr11:18824400-18824600	Bivalent/Poised TSS	Fetal Lung	lung
37	chr11:18824400-18824600	Enhancers	NHEK	skin
38	chr11:18824400-18824800	Enhancers	Stomach Mucosa	stomach
39	chr11:18824400-18825000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr11:18824600-18824800	Active TSS	Brain Anterior Caudate	brain
41	chr11:18824600-18824800	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr11:18824600-18825400	Enhancers	HMEC	breast
43	chr11:18824800-18826000	Weak transcription	NHEK	skin
44	chr11:18825000-18825600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr11:18825400-18825800	Weak transcription	HMEC	breast
46	chr11:18825600-18826600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr11:18825800-18826600	Enhancers	HMEC	breast
48	chr11:18826000-18826600	Enhancers	NHEK	skin
49	chr11:18826600-18828000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr11:18828000-18828200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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