Variant report

Variant	esv1825024
Chromosome Location	chr2:127798138-127864285
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2283)
CpG islands
(count:1954)
Chromatin interactive
region (count:92)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2283 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:127822615-127822618	K562	blood:	n/a	n/a
2	ARID3A	chr2:127807793-127807989	HepG2	liver:	n/a	n/a
3	ATF2	chr2:127825494-127825920	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr2:127844429-127844950	GM12878	blood:	n/a	n/a
5	ATF2	chr2:127844404-127844947	GM12878	blood:	n/a	n/a
6	ATF2	chr2:127839350-127839700	GM12878	blood:	n/a	n/a
7	ATF2	chr2:127825499-127825993	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr2:127822206-127822801	K562	blood:	n/a	n/a
9	ATF3	chr2:127822130-127822684	K562	blood:	n/a	n/a
10	ATF3	chr2:127825591-127825922	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr2:127822254-127822814	A549	lung:	n/a	n/a
12	ATF3	chr2:127825607-127825875	K562	blood:	n/a	n/a
13	BACH1	chr2:127822214-127822973	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:127822234-127822731	K562	blood:	n/a	n/a
15	BACH1	chr2:127807740-127808003	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr2:127863286-127863726	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr2:127802018-127802163	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr2:127825651-127825951	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr2:127846567-127846639	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr2:127822263-127822708	GM12878	blood:	n/a	chr2:127822516-127822527 chr2:127822517-127822527
21	BCL11A	chr2:127844549-127844858	GM12878	blood:	n/a	n/a
22	BCL3	chr2:127807664-127808252	A549	lung:	n/a	n/a
23	BCL3	chr2:127811506-127811950	GM12878	blood:	n/a	n/a
24	BCL3	chr2:127822265-127822701	K562	blood:	n/a	n/a
25	BCL3	chr2:127801087-127802446	GM12878	blood:	n/a	n/a
26	BCL3	chr2:127811578-127811877	GM12878	blood:	n/a	n/a
27	BCL3	chr2:127801129-127802418	GM12878	blood:	n/a	n/a
28	BCL3	chr2:127821940-127822838	A549	lung:	n/a	chr2:127822050-127822059
29	BCLAF1	chr2:127822262-127822771	K562	blood:	n/a	n/a
30	BCLAF1	chr2:127822359-127822805	GM12878	blood:	n/a	n/a
31	BCLAF1	chr2:127839268-127839716	GM12878	blood:	n/a	n/a
32	BCLAF1	chr2:127844359-127844791	GM12878	blood:	n/a	n/a
33	BCLAF1	chr2:127825630-127825900	GM12878	blood:	n/a	n/a
34	BCLAF1	chr2:127822259-127822834	K562	blood:	n/a	n/a
35	BHLHE40	chr2:127825293-127825973	K562	blood:	n/a	n/a
36	BHLHE40	chr2:127807725-127808031	K562	blood:	n/a	chr2:127807929-127807945
37	BHLHE40	chr2:127838526-127839961	GM12878	blood:	n/a	n/a
38	BHLHE40	chr2:127844529-127844581	K562	blood:	n/a	n/a
39	BHLHE40	chr2:127804192-127804461	HepG2	liver:	n/a	chr2:127804298-127804307
40	BHLHE40	chr2:127842880-127843222	GM12878	blood:	n/a	n/a
41	BHLHE40	chr2:127844445-127844936	GM12878	blood:	n/a	n/a
42	BHLHE40	chr2:127822136-127823109	K562	blood:	n/a	n/a
43	BHLHE40	chr2:127841796-127841981	K562	blood:	n/a	n/a
44	BHLHE40	chr2:127810784-127810984	K562	blood:	n/a	n/a
45	BHLHE40	chr2:127804120-127804413	GM12878	blood:	n/a	chr2:127804298-127804307
46	BHLHE40	chr2:127822373-127822818	GM12878	blood:	n/a	n/a
47	BHLHE40	chr2:127825347-127825940	GM12878	blood:	n/a	n/a
48	BHLHE40	chr2:127823468-127823585	K562	blood:	n/a	n/a
49	BHLHE40	chr2:127825385-127825984	HepG2	liver:	n/a	n/a
50	BHLHE40	chr2:127804162-127804488	K562	blood:	n/a	chr2:127804298-127804307

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:127818000-127818050	Caco-2	colon:	n/a
2	chr2:127862614-127862664	MCF10A-Er-Src	breast:	n/a
3	chr2:127818000-127818050	Caco-2	colon:	n/a
4	chr2:127862614-127862664	MCF10A-Er-Src	breast:	n/a
5	chr2:127826149-127826199	Caco-2	colon:	n/a
6	chr2:127826149-127826199	H1-hESC	embryonic stem cell:	embryo
7	chr2:127811805-127811855	HCPEpiC	choroid plexus:	n/a
8	chr2:127863656-127863706	GM19239	blood:	n/a
9	chr2:127815133-127815183	AG10803	skin:	n/a
10	chr2:127863656-127863706	NHBE	bronchial:	n/a
11	chr2:127801271-127801321	PANC-1	pancreas:	n/a
12	chr2:127826149-127826199	PANC-1	pancreas:	n/a
13	chr2:127815133-127815183	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:127818131-127818181	Hela-S3	cervix:	n/a
15	chr2:127818131-127818181	NH-A	brain:	n/a
16	chr2:127826149-127826199	GM19239	blood:	n/a
17	chr2:127826149-127826199	HCF	heart:	n/a
18	chr2:127801137-127801187	HAEpiC	amniotic membrane:	n/a
19	chr2:127852450-127852500	GM12878	blood:	n/a
20	chr2:127841945-127841995	SK-N-SH	brain:	n/a
21	chr2:127852450-127852500	NHDF-neo	bronchial:	n/a
22	chr2:127815133-127815183	HCT-116	colon:	n/a
23	chr2:127852450-127852500	NHBE	bronchial:	n/a
24	chr2:127864026-127864076	HCT-116	colon:	n/a
25	chr2:127861092-127861142	PrEC	prostate:	n/a
26	chr2:127862614-127862664	HepG2	liver:	n/a
27	chr2:127805770-127805820	NH-A	brain:	n/a
28	chr2:127825935-127825985	RPTEC	kidney:	n/a
29	chr2:127805855-127805905	IMR90	lung:	fetal
30	chr2:127830703-127830753	H1-hESC	embryonic stem cell:	embryo
31	chr2:127815206-127815256	AoSMC	blood vessel:	n/a
32	chr2:127825935-127825985	AG04450	lung:	fetal
33	chr2:127818131-127818181	T-47D	breast:	n/a
34	chr2:127811805-127811855	NH-A	brain:	n/a
35	chr2:127811805-127811855	AG10803	skin:	n/a
36	chr2:127805910-127805960	HCT-116	colon:	n/a
37	chr2:127841945-127841995	IMR90	lung:	fetal
38	chr2:127805910-127805960	Hepatocyte	liver:	n/a
39	chr2:127864026-127864076	GM12892	blood:	n/a
40	chr2:127801271-127801321	NHBE	bronchial:	n/a
41	chr2:127862614-127862664	NHDF-neo	bronchial:	n/a
42	chr2:127839539-127839589	CMK	blood:	n/a
43	chr2:127862614-127862664	HRCEpiC	kidney:	n/a
44	chr2:127800646-127800696	SK-N-SH_RA	brain:	n/a
45	chr2:127825935-127825985	SKMC	muscle:	n/a
46	chr2:127815206-127815256	HIPEpiC	eye:	n/a
47	chr2:127863656-127863706	HAEpiC	amniotic membrane:	n/a
48	chr2:127800646-127800696	SAEC	small airway:	n/a
49	chr2:127830703-127830753	AG04449	skin:	fetal
50	chr2:127800616-127800666	Jurkat	blood:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:127825662..127826505-chr2:127954218..127955183,2	MCF-7	breast:
2	chr2:127853337..127855770-chr2:127871735..127873345,2	K562	blood:
3	chr2:127842254..127844330-chr2:127859021..127861716,3	MCF-7	breast:
4	chr2:127812772..127815710-chr2:127817588..127820461,3	K562	blood:
5	chr2:127815347..127818543-chr2:127821043..127823308,3	K562	blood:
6	chr2:127834991..127836623-chr2:127840456..127842151,2	MCF-7	breast:
7	chr2:127840601..127843824-chr2:127844844..127848160,4	K562	blood:
8	chr2:127825705..127826883-chr2:127897059..127898198,8	MCF-7	breast:
9	chr2:127837291..127839948-chr2:127841422..127844629,3	K562	blood:
10	chr2:127842254..127844330-chr2:127859021..127861716,3	MCF-7	breast:
11	chr2:127813553..127815177-chr2:127820446..127822528,2	MCF-7	breast:
12	chr2:127812073..127814969-chr2:127823629..127825354,2	K562	blood:
13	chr2:127812299..127814743-chr2:127815692..127817435,2	MCF-7	breast:
14	chr2:127834701..127837421-chr2:127840734..127842424,2	MCF-7	breast:
15	chr2:127823166..127825424-chr2:127856557..127859034,2	MCF-7	breast:
16	chr2:127810346..127812900-chr2:127820941..127823666,3	MCF-7	breast:
17	chr2:127822004..127823991-chr2:127859645..127861835,2	MCF-7	breast:
18	chr2:127829446..127832299-chr2:127837118..127839537,2	K562	blood:
19	chr2:127822177..127823094-chr7:128694437..128695276,2	Hela-S3	cervix:
20	chr2:127825650..127826234-chr2:127897075..127897865,2	MCF-7	breast:
21	chr2:127834991..127836623-chr2:127840456..127842151,2	MCF-7	breast:
22	chr2:127782007..127782956-chr2:127806151..127807307,3	MCF-7	breast:
23	chr2:127846711..127850055-chr2:127853164..127855548,3	MCF-7	breast:
24	chr2:127846711..127850055-chr2:127853164..127855548,3	MCF-7	breast:
25	chr2:127807319..127809537-chr2:127812117..127815933,4	MCF-7	breast:
26	chr2:127839430..127842816-chr2:127848432..127852029,4	MCF-7	breast:
27	chr2:127841990..127844933-chr2:127856467..127858298,2	K562	blood:
28	chr2:127825712..127826261-chr2:127901784..127902300,2	MCF-7	breast:
29	chr2:127822672..127825565-chr2:127830790..127832845,2	K562	blood:
30	chr2:127729704..127730234-chr2:127807453..127808173,2	K562	blood:
31	chr2:127805679..127808550-chr2:127820998..127823785,2	MCF-7	breast:
32	chr2:127823166..127825424-chr2:127856557..127859034,2	MCF-7	breast:
33	chr2:127809898..127812598-chr2:127812721..127816309,3	MCF-7	breast:
34	chr2:127841990..127844933-chr2:127856467..127858298,2	K562	blood:
35	chr2:127854702..127856656-chr2:127856950..127858701,2	MCF-7	breast:
36	chr2:127819816..127822749-chr2:127823381..127826394,3	K562	blood:
37	chr2:127818793..127821567-chr2:127826127..127828276,2	MCF-7	breast:
38	chr2:127002328..127003186-chr2:127807433..127808421,2	K562	blood:
39	chr2:127837291..127839948-chr2:127841422..127844629,3	K562	blood:
40	chr2:127800876..127803938-chr2:127806149..127808710,3	MCF-7	breast:
41	chr2:127837345..127839578-chr2:127840445..127843454,3	MCF-7	breast:
42	chr2:127781170..127783496-chr2:127799627..127801145,2	K562	blood:
43	chr2:127808007..127810886-chr2:127814452..127816219,3	K562	blood:
44	chr2:127808007..127810886-chr2:127814452..127816219,3	K562	blood:
45	chr2:127844458..127846446-chr2:127850246..127851813,2	K562	blood:
46	chr2:127840601..127843824-chr2:127844844..127848160,4	K562	blood:
47	chr2:127829694..127830341-chr2:127897153..127898129,2	MCF-7	breast:
48	chr2:127820803..127824621-chr2:127824894..127830047,6	K562	blood:
49	chr2:127825324..127826896-chr2:127856890..127859750,2	MCF-7	breast:
50	chr2:127825324..127826896-chr2:127856890..127859750,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC114783.1.1-4	chr2:127863176-127863231	NONHSAT074143
2	lnc-AC114783.1.1-4	chr2:127862718-127863044	l_1944_chr2:127862717-127879890_lung
3	lnc-CYP27C1-1	chr2:127861773-127862104	expReg_chr2_9105_-
4	lnc-AC114783.1.1-4	chr2:127863157-127863231	l_1944_chr2:127862717-127879890_lung

No data

Variant related genes	Relation type
BIN1	TF binding region
BIN1	CpG island
ENSG00000169967	chromatin interactions
ENSG00000064419	chromatin interactions
ENSG00000260163	chromatin interactions
ENSG00000260634	chromatin interactions
ENSG00000136717	chromatin interactions

Extended variants
information (count: 3015 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3015 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533377794	chr2:127798159-127798160	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs79709157	chr2:127798170-127798171	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530064365	chr2:127798225-127798226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535210461	chr2:127798231-127798232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555299473	chr2:127798238-127798239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10929004	chr2:127798270-127798271	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs534902700	chr2:127798274-127798275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558117053	chr2:127798278-127798279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146840902	chr2:127798285-127798286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541825707	chr2:127798290-127798291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543613488	chr2:127798303-127798304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112641008	chr2:127798306-127798307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369013644	chr2:127798325-127798326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146433041	chr2:127798326-127798327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183223691	chr2:127798352-127798353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541960837	chr2:127798355-127798356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562105036	chr2:127798421-127798422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563307035	chr2:127798437-127798438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs13417782	chr2:127798438-127798439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534873022	chr2:127798448-127798449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187936135	chr2:127798459-127798460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564412655	chr2:127798463-127798464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191698347	chr2:127798464-127798465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550310559	chr2:127798469-127798470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543129990	chr2:127798487-127798488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570160962	chr2:127798522-127798523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530537354	chr2:127798541-127798542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183528877	chr2:127798550-127798551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188784098	chr2:127798554-127798555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192665606	chr2:127798583-127798584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373912428	chr2:127798608-127798609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571531131	chr2:127798609-127798610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537350817	chr2:127798685-127798686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377751316	chr2:127798736-127798737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557072104	chr2:127798757-127798758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140775858	chr2:127798782-127798783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369536418	chr2:127798783-127798784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551960694	chr2:127798833-127798834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150119273	chr2:127798856-127798857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74857928	chr2:127798904-127798905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564151582	chr2:127798908-127798909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577871091	chr2:127799026-127799027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183436244	chr2:127799064-127799065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145493049	chr2:127799100-127799101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75390896	chr2:127799101-127799102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201149188	chr2:127799124-127799125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549038859	chr2:127799150-127799151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570533449	chr2:127799152-127799153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186635328	chr2:127799153-127799154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs528936151	chr2:127799176-127799177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	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
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Mental retardation	17621639	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Medulloblastoma	16968546	CNVD
Neurocytoma	17123091	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3196 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127783800-127815600	Weak transcription	Aorta	Aorta
2	chr2:127793200-127801200	Weak transcription	Fetal Lung	lung
3	chr2:127793200-127805400	Weak transcription	Liver	Liver
4	chr2:127795600-127801400	Weak transcription	Fetal Heart	heart
5	chr2:127795800-127807600	Weak transcription	Brain Germinal Matrix	brain
6	chr2:127797400-127798200	Enhancers	GM12878-XiMat	blood
7	chr2:127797600-127798200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:127797600-127805200	Weak transcription	Primary B cells from peripheral blood	blood
9	chr2:127797800-127803600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:127797800-127805600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr2:127798200-127799200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr2:127798200-127811400	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr2:127799000-127799800	Enhancers	Brain Cingulate Gyrus	brain
14	chr2:127799200-127799400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:127799200-127799400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
16	chr2:127799200-127799400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr2:127799200-127799800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr2:127799400-127799600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:127799400-127799600	Enhancers	Brain Angular Gyrus	brain
20	chr2:127799400-127799600	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr2:127799400-127799600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr2:127799400-127799600	Enhancers	Right Ventricle	heart
23	chr2:127799400-127799800	Enhancers	Fetal Kidney	kidney
24	chr2:127799400-127801400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:127799400-127804800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr2:127799600-127801800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr2:127799600-127803800	Weak transcription	Right Ventricle	heart
28	chr2:127799600-127805800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr2:127799600-127805800	Weak transcription	Gastric	stomach
30	chr2:127799600-127806200	Weak transcription	Brain Angular Gyrus	brain
31	chr2:127799800-127800600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr2:127799800-127801200	Weak transcription	Fetal Kidney	kidney
33	chr2:127800000-127807600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr2:127800200-127807400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr2:127800400-127800600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:127800400-127802000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr2:127800600-127801400	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr2:127800600-127801400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr2:127801200-127801400	Enhancers	Esophagus	oesophagus
40	chr2:127801200-127801400	Enhancers	Fetal Lung	lung
41	chr2:127801200-127801400	Weak transcription	Pancreas	Pancrea
42	chr2:127801200-127801600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr2:127801200-127802400	ZNF genes & repeats	Fetal Kidney	kidney
44	chr2:127801200-127806000	Weak transcription	NHLF	lung
45	chr2:127801400-127801600	ZNF genes & repeats	Fetal Heart	heart
46	chr2:127801400-127801600	Flanking Active TSS	Fetal Lung	lung
47	chr2:127801400-127801800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:127801400-127801800	ZNF genes & repeats	Pancreas	Pancrea
49	chr2:127801400-127801800	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr2:127801400-127802200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell

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