Variant report

Variant	esv2758220
Chromosome Location	chr10:55360612-55586930
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	chr10:55546113-55546324	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:55379164-55379197	K562	blood:	n/a	n/a
3	ARID3A	chr10:55361088-55361391	HepG2	liver:	n/a	n/a
4	BACH1	chr10:55410674-55410823	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr10:55436651-55436653	Hela-S3	cervix:	n/a	n/a
6	CCNT2	chr10:55407553-55407753	K562	blood:	n/a	n/a
7	CEBPB	chr10:55456808-55457116	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr10:55440212-55440489	A549	lung:	n/a	chr10:55440348-55440359
9	CEBPB	chr10:55531808-55532061	HepG2	liver:	n/a	chr10:55531918-55531929
10	CEBPB	chr10:55411759-55412117	Hela-S3	cervix:	n/a	chr10:55411925-55411936
11	CEBPB	chr10:55495099-55495137	K562	blood:	n/a	n/a
12	CEBPB	chr10:55495107-55495314	A549	lung:	n/a	n/a
13	CEBPB	chr10:55482323-55482573	IMR90	lung:	n/a	chr10:55482450-55482463 chr10:55482451-55482462 chr10:55482452-55482461 chr10:55482452-55482461 chr10:55482450-55482461 chr10:55482452-55482461 chr10:55482450-55482463 chr10:55482452-55482461 chr10:55482450-55482463
14	CEBPB	chr10:55484473-55484797	IMR90	lung:	n/a	chr10:55484642-55484651 chr10:55484640-55484651 chr10:55484642-55484653 chr10:55484640-55484653
15	CEBPB	chr10:55440562-55440588	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr10:55440217-55440437	IMR90	lung:	n/a	chr10:55440348-55440359
17	CEBPB	chr10:55484526-55484810	A549	lung:	n/a	chr10:55484642-55484651 chr10:55484640-55484651 chr10:55484642-55484653 chr10:55484640-55484653
18	CEBPB	chr10:55573444-55573642	HepG2	liver:	n/a	chr10:55573508-55573519
19	CEBPB	chr10:55361129-55361360	A549	lung:	n/a	n/a
20	CEBPB	chr10:55482351-55482593	HepG2	liver:	n/a	chr10:55482450-55482463 chr10:55482451-55482462 chr10:55482452-55482461 chr10:55482452-55482461 chr10:55482450-55482461 chr10:55482452-55482461 chr10:55482450-55482463 chr10:55482452-55482461 chr10:55482450-55482463
21	CEBPB	chr10:55577616-55577876	HepG2	liver:	n/a	n/a
22	CEBPB	chr10:55539511-55539751	HepG2	liver:	n/a	n/a
23	CEBPB	chr10:55494993-55495303	IMR90	lung:	n/a	n/a
24	CEBPB	chr10:55407097-55407340	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr10:55572413-55572622	H1-hESC	embryonic stem cell:	n/a	chr10:55572521-55572530 chr10:55572521-55572530 chr10:55572519-55572532 chr10:55572521-55572530
26	CEBPB	chr10:55484474-55484818	HepG2	liver:	n/a	chr10:55484642-55484651 chr10:55484640-55484651 chr10:55484642-55484653 chr10:55484640-55484653
27	CEBPB	chr10:55495022-55495339	HepG2	liver:	n/a	n/a
28	CEBPB	chr10:55572397-55572600	HepG2	liver:	n/a	chr10:55572521-55572530 chr10:55572521-55572530 chr10:55572519-55572532 chr10:55572521-55572530
29	CEBPB	chr10:55440189-55440480	HepG2	liver:	n/a	chr10:55440348-55440359
30	CEBPB	chr10:55531788-55532061	IMR90	lung:	n/a	chr10:55531918-55531929
31	CEBPB	chr10:55411770-55412027	HepG2	liver:	n/a	chr10:55411925-55411936
32	CEBPB	chr10:55531778-55532075	H1-hESC	embryonic stem cell:	n/a	chr10:55531918-55531929
33	CHD1	chr10:55509966-55509970	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr10:55361120-55361270	MCF-7	breast:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
35	CTCF	chr10:55361065-55361505	MCF-7	breast:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
36	CTCF	chr10:55361120-55361270	GM12873	blood:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
37	CTCF	chr10:55546100-55546250	GM12878	blood:	n/a	n/a
38	CTCF	chr10:55546120-55546270	GM12865	blood:	n/a	n/a
39	CTCF	chr10:55546100-55546250	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr10:55546058-55546349	K562	blood:	n/a	n/a
41	CTCF	chr10:55361140-55361290	GM12869	blood:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
42	CTCF	chr10:55361120-55361270	SAEC	small airway:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
43	CTCF	chr10:55361160-55361310	AG09309	skin:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
44	CTCF	chr10:55546020-55546170	HMEC	breast:	n/a	n/a
45	CTCF	chr10:55546100-55546250	HPF	lung:	n/a	n/a
46	CTCF	chr10:55546038-55546322	Gliobla	brain:	n/a	n/a
47	CTCF	chr10:55546140-55546290	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr10:55568620-55568677	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr10:55361140-55361290	HMEC	breast:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234
50	CTCF	chr10:55361180-55361330	HA-sp	spinal cord:	n/a	chr10:55361218-55361239 chr10:55361217-55361233 chr10:55361216-55361234

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55419714-55419764	HUVEC	blood vessel:	n/a
2	chr10:55419927-55419977	HL-60	blood:	n/a
3	chr10:55419714-55419764	HUVEC	blood vessel:	n/a
4	chr10:55419927-55419977	HL-60	blood:	n/a
5	chr10:55419927-55419977	MCF10A-Er-Src	breast:	n/a
6	chr10:55568997-55569047	ECC-1	luminal epithelium:	n/a
7	chr10:55419714-55419764	GM06990	blood:	n/a
8	chr10:55419714-55419764	ovcar-3	ovarian:	n/a
9	chr10:55419927-55419977	GM12891	blood:	n/a
10	chr10:55393450-55393500	GM12891	blood:	n/a
11	chr10:55419714-55419764	HAEpiC	amniotic membrane:	n/a
12	chr10:55419927-55419977	BE2_C	brain:	n/a
13	chr10:55568997-55569047	Hela-S3	cervix:	n/a
14	chr10:55419927-55419977	HEK293	kidney:	embryo
15	chr10:55393450-55393500	HUVEC	blood vessel:	n/a
16	chr10:55568997-55569047	Hepatocyte	liver:	n/a
17	chr10:55419927-55419977	SAEC	small airway:	n/a
18	chr10:55419714-55419764	GM19239	blood:	n/a
19	chr10:55568997-55569047	HPAEpiC	pulmonary alveolar:	n/a
20	chr10:55393450-55393500	Hela-S3	cervix:	n/a
21	chr10:55393450-55393500	HL-60	blood:	n/a
22	chr10:55393450-55393500	HCF	heart:	n/a
23	chr10:55568997-55569047	HEK293	kidney:	embryo
24	chr10:55393450-55393500	HCT-116	colon:	n/a
25	chr10:55393450-55393500	HRPEpiC	eye:	n/a
26	chr10:55419714-55419764	HEK293	kidney:	embryo
27	chr10:55393450-55393500	MCF-7	breast:	n/a
28	chr10:55419927-55419977	GM06990	blood:	n/a
29	chr10:55393450-55393500	SK-N-SH_RA	brain:	n/a
30	chr10:55419714-55419764	SAEC	small airway:	n/a
31	chr10:55419927-55419977	SKMC	muscle:	n/a
32	chr10:55419927-55419977	HCT-116	colon:	n/a
33	chr10:55419714-55419764	A549	lung:	n/a
34	chr10:55419714-55419764	NH-A	brain:	n/a
35	chr10:55568997-55569047	GM19239	blood:	n/a
36	chr10:55568997-55569047	HAEpiC	amniotic membrane:	n/a
37	chr10:55419714-55419764	SKMC	muscle:	n/a
38	chr10:55419714-55419764	HL-60	blood:	n/a
39	chr10:55419927-55419977	PFSK-1	brain:	n/a
40	chr10:55393450-55393500	U87	brain:	n/a
41	chr10:55393450-55393500	PANC-1	pancreas:	n/a
42	chr10:55393450-55393500	T-47D	breast:	n/a
43	chr10:55393450-55393500	AG09319	gingival:	n/a
44	chr10:55419714-55419764	NT2-D1	testis:	n/a
45	chr10:55568997-55569047	T-47D	breast:	n/a
46	chr10:55568997-55569047	NHBE	bronchial:	n/a
47	chr10:55419714-55419764	K562	blood:	n/a
48	chr10:55393450-55393500	HIPEpiC	eye:	n/a
49	chr10:55419714-55419764	Caco-2	colon:	n/a
50	chr10:55419927-55419977	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:55057963..55058535-chr10:55568196..55569129,2	MCF-7	breast:
2	chr10:55558585..55559152-chr17:58469714..58470538,2	MCF-7	breast:
3	chr10:55481740..55482260-chr20:52673713..52674214,2	MCF-7	breast:
4	chr10:55360709..55361787-chr10:55606233..55607054,5	MCF-7	breast:
5	chr10:55466040..55468835-chr10:55471879..55474110,2	K562	blood:
6	chr10:55549906..55552050-chr10:55558959..55560597,2	K562	blood:
7	chr10:55549906..55552050-chr10:55558959..55560597,2	K562	blood:
8	10:55527193-55535408..10:55949104-55956834	K562	blood:
9	chr10:55360883..55361625-chr10:55568215..55569121,2	MCF-7	breast:
10	chr10:55466040..55468835-chr10:55471879..55474110,2	K562	blood:
11	chr10:55405153..55407581-chr5:63345532..63348450,2	MCF-7	breast:
12	chr10:55360883..55361625-chr10:55568215..55569121,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DKK1-4	chr10:55526160-55526374	NONHSAT013453

Variant related genes	Relation type
PCDH15	TF binding region
ENSG00000233805	TF binding region
PCDH15	CpG island
ENSG00000233805	CpG island
ENSG00000170832	chromatin interactions
ENSG00000141371	chromatin interactions

Extended variants
information (count: 4133 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:4133 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183936804	chr10:55360644-55360645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546063217	chr10:55360702-55360703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575155429	chr10:55360703-55360704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557076548	chr10:55360705-55360706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188834175	chr10:55360706-55360707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4935081	chr10:55360806-55360807	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs373553201	chr10:55360809-55360810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572991611	chr10:55360811-55360812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141366863	chr10:55360875-55360876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541615863	chr10:55360957-55360958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7093101	chr10:55360972-55360973	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs115255164	chr10:55360977-55360978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530589279	chr10:55361017-55361018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541064929	chr10:55361047-55361048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192545629	chr10:55361081-55361082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577671536	chr10:55361103-55361104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184353724	chr10:55361117-55361118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563873548	chr10:55361120-55361121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550619833	chr10:55361172-55361173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370852430	chr10:55361190-55361191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543285291	chr10:55361210-55361211	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs560123885	chr10:55361271-55361272	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs528090618	chr10:55361366-55361367	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs551348985	chr10:55361371-55361372	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs187133474	chr10:55361373-55361374	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs571272252	chr10:55361391-55361392	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs530591805	chr10:55361457-55361458	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs550424443	chr10:55361465-55361466	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs562817202	chr10:55361466-55361467	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs536089887	chr10:55361512-55361513	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs553220680	chr10:55361513-55361514	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs566480068	chr10:55361520-55361521	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs535852561	chr10:55361559-55361560	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs145096414	chr10:55361573-55361574	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs200679633	chr10:55361579-55361580	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs531584772	chr10:55361626-55361627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191902265	chr10:55361635-55361636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369134466	chr10:55361643-55361644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557202721	chr10:55361673-55361674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574161774	chr10:55361689-55361690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532887257	chr10:55361692-55361693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184459535	chr10:55361714-55361715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188973518	chr10:55361729-55361730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181794284	chr10:55361730-55361731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs151337957	chr10:55361761-55361762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368938748	chr10:55361821-55361822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185535413	chr10:55361837-55361838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190402721	chr10:55361945-55361946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9733895	chr10:55361947-55361948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs180890049	chr10:55361967-55361968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Intellectual disability	21948486	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Colorectal cancer	16774939	CNVD
Autism	20858243	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Usher type I cohort	17277737	CNVD
Usher type I cohort	21436283	CNVD
Leukemia	21357790	CNVD
Medulloblastoma	22832581	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:215 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55357600-55361000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr10:55359200-55361200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr10:55359600-55360800	Weak transcription	NHEK	skin
4	chr10:55359600-55362200	Weak transcription	HMEC	breast
5	chr10:55359600-55366800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr10:55359800-55361400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr10:55359800-55362400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr10:55360200-55361400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr10:55360600-55360800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr10:55360600-55361200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr10:55360800-55361600	Enhancers	NHEK	skin
12	chr10:55360800-55367400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr10:55361000-55361200	Enhancers	Placenta Amnion	Placenta Amnion
14	chr10:55361200-55361400	Active TSS	Liver	Liver
15	chr10:55361200-55361400	Enhancers	HUVEC	blood vessel
16	chr10:55361200-55361600	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr10:55361200-55362800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr10:55361200-55365800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr10:55361400-55361600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr10:55361400-55361600	Flanking Active TSS	Liver	Liver
21	chr10:55361400-55361600	Enhancers	Stomach Mucosa	stomach
22	chr10:55361400-55367000	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr10:55361600-55362000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr10:55362000-55362200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr10:55362200-55362400	Enhancers	HMEC	breast
26	chr10:55362200-55371400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr10:55362400-55362600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr10:55365200-55365400	Enhancers	Fetal Lung	lung
29	chr10:55365400-55366000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr10:55365400-55366000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr10:55365400-55366000	Enhancers	H9 Cell Line	embryonic stem cell
32	chr10:55365400-55366800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr10:55365600-55366000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr10:55365600-55367200	Weak transcription	Fetal Lung	lung
35	chr10:55365800-55366200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr10:55366000-55371200	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr10:55366200-55366400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr10:55366400-55368200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr10:55366600-55368200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr10:55366800-55367000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr10:55366800-55368000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr10:55367000-55367400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr10:55367000-55368000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr10:55367200-55368600	Enhancers	Fetal Lung	lung
45	chr10:55367400-55367800	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr10:55367400-55367800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr10:55367800-55376600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr10:55368000-55373200	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr10:55368000-55379000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr10:55368200-55373200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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