Variant report

Variant	nsv895405
Chromosome Location	chr10:54765608-54824741
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:262)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:54812645-54812845	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:54766296-54767482	HepG2	liver:	n/a	n/a
3	ATF2	chr10:54782216-54782718	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr10:54782245-54782835	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr10:54773034-54773276	GM12878	blood:	n/a	n/a
6	BCL11A	chr10:54782292-54782638	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr10:54782709-54782744	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:54789662-54789889	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:54766801-54767080	HepG2	liver:	n/a	n/a
10	BHLHE40	chr10:54772825-54773371	GM12878	blood:	n/a	n/a
11	BHLHE40	chr10:54765171-54765964	GM12878	blood:	n/a	chr10:54765555-54765568 chr10:54765557-54765566 chr10:54765556-54765565 chr10:54765551-54765572
12	CEBPB	chr10:54798877-54799130	HepG2	liver:	n/a	chr10:54798994-54799005 chr10:54798993-54799006 chr10:54798978-54798989
13	CEBPB	chr10:54802424-54802606	IMR90	lung:	n/a	n/a
14	CEBPB	chr10:54812569-54812835	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:54802374-54802596	HepG2	liver:	n/a	chr10:54802395-54802407
16	CEBPB	chr10:54766710-54767059	HepG2	liver:	n/a	n/a
17	CEBPB	chr10:54798974-54799011	IMR90	lung:	n/a	chr10:54798994-54799005 chr10:54798993-54799006 chr10:54798978-54798989
18	CEBPB	chr10:54806095-54806330	HepG2	liver:	n/a	chr10:54806203-54806216 chr10:54806204-54806215 chr10:54806203-54806214 chr10:54806203-54806216
19	CEBPB	chr10:54790215-54790565	IMR90	lung:	n/a	n/a
20	CHD2	chr10:54789549-54789899	GM12878	blood:	n/a	n/a
21	CHD2	chr10:54812157-54812247	HepG2	liver:	n/a	n/a
22	CTCF	chr10:54799346-54799409	GM10248	blood:	n/a	n/a
23	CTCF	chr10:54820034-54820118	GM20000	blood:	n/a	n/a
24	CTCF	chr10:54795020-54795170	GM12869	blood:	n/a	n/a
25	CTCF	chr10:54788501-54788615	GM19238	blood:	n/a	n/a
26	CTCF	chr10:54788566-54788619	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr10:54788534-54788584	HepG2	liver:	n/a	n/a
28	CTCF	chr10:54788534-54788565	GM19240	blood:	n/a	n/a
29	CTCF	chr10:54782680-54782830	Caco-2	colon:	n/a	n/a
30	CTCF	chr10:54782440-54782590	Caco-2	colon:	n/a	n/a
31	CTCF	chr10:54788549-54788553	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr10:54770400-54770550	AG10803	skin:	n/a	n/a
33	CUX1	chr10:54818130-54818131	GM12878	blood:	n/a	n/a
34	CUX1	chr10:54772800-54773567	GM12878	blood:	n/a	n/a
35	E2F4	chr10:54794671-54794808	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr10:54802182-54802408	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F6	chr10:54789198-54789460	H1-hESC	embryonic stem cell:	n/a	n/a
38	E2F6	chr10:54789184-54790029	H1-hESC	embryonic stem cell:	n/a	n/a
39	EBF1	chr10:54775757-54775897	GM12878	blood:	n/a	n/a
40	EBF1	chr10:54773077-54773453	GM12878	blood:	n/a	n/a
41	EBF1	chr10:54776847-54776886	GM12878	blood:	n/a	n/a
42	EBF1	chr10:54789785-54789872	GM12878	blood:	n/a	n/a
43	EBF1	chr10:54776657-54776891	GM12878	blood:	n/a	chr10:54776786-54776795 chr10:54776784-54776797 chr10:54776786-54776795 chr10:54776786-54776796
44	EP300	chr10:54782275-54782782	ECC-1	luminal epithelium:	n/a	n/a
45	EP300	chr10:54766749-54767102	HepG2	liver:	n/a	n/a
46	EP300	chr10:54766590-54767109	HepG2	liver:	n/a	n/a
47	EP300	chr10:54824397-54824722	GM12878	blood:	n/a	n/a
48	EP300	chr10:54772964-54773391	GM12878	blood:	n/a	chr10:54773097-54773106 chr10:54773064-54773078
49	EP300	chr10:54765363-54765652	GM12878	blood:	n/a	n/a
50	EP300	chr10:54766536-54767205	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:54782631-54782681	NHDF-neo	bronchial:	n/a
2	chr10:54782631-54782681	HMEC	breast:	n/a
3	chr10:54782631-54782681	SK-N-SH	brain:	n/a
4	chr10:54782631-54782681	GM06990	blood:	n/a
5	chr10:54782631-54782681	AG09309	skin:	n/a
6	chr10:54782631-54782681	RPTEC	kidney:	n/a
7	chr10:54782631-54782681	T-47D	breast:	n/a
8	chr10:54782631-54782681	SK-N-MC	brain:	n/a
9	chr10:54782631-54782681	HCPEpiC	choroid plexus:	n/a
10	chr10:54782631-54782681	ECC-1	luminal epithelium:	n/a
11	chr10:54782631-54782681	H1-hESC	embryonic stem cell:	embryo
12	chr10:54782631-54782681	GM12891	blood:	n/a
13	chr10:54782631-54782681	HRE	kidney:	n/a
14	chr10:54782631-54782681	BJ	skin:	n/a
15	chr10:54782631-54782681	NT2-D1	testis:	n/a
16	chr10:54782631-54782681	Caco-2	colon:	n/a
17	chr10:54782631-54782681	GM19239	blood:	n/a
18	chr10:54782631-54782681	HCT-116	colon:	n/a
19	chr10:54782631-54782681	U87	brain:	n/a
20	chr10:54782631-54782681	ovcar-3	ovarian:	n/a
21	chr10:54782631-54782681	HNPCEpiC	eye:	n/a
22	chr10:54782631-54782681	GM12892	blood:	n/a
23	chr10:54782631-54782681	HRPEpiC	eye:	n/a
24	chr10:54782631-54782681	HEEpiC	esophagus:	n/a
25	chr10:54782631-54782681	SKMC	muscle:	n/a
26	chr10:54782631-54782681	NB4	blood:	n/a
27	chr10:54782631-54782681	AG10803	skin:	n/a
28	chr10:54782631-54782681	HAEpiC	amniotic membrane:	n/a
29	chr10:54782631-54782681	Hepatocyte	liver:	n/a
30	chr10:54782631-54782681	ProgFib	skin:	n/a
31	chr10:54782631-54782681	HCM	heart:	n/a
32	chr10:54782631-54782681	AG04449	skin:	fetal
33	chr10:54782631-54782681	A549	lung:	n/a
34	chr10:54782631-54782681	AoSMC	blood vessel:	n/a
35	chr10:54782631-54782681	K562	blood:	n/a
36	chr10:54782631-54782681	Hela-S3	cervix:	n/a
37	chr10:54782631-54782681	AG04450	lung:	fetal
38	chr10:54782631-54782681	HUVEC	blood vessel:	n/a
39	chr10:54782631-54782681	PrEC	prostate:	n/a
40	chr10:54782631-54782681	NHBE	bronchial:	n/a
41	chr10:54782631-54782681	HPAEpiC	pulmonary alveolar:	n/a
42	chr10:54782631-54782681	PANC-1	pancreas:	n/a
43	chr10:54782631-54782681	NH-A	brain:	n/a
44	chr10:54782631-54782681	HCF	heart:	n/a
45	chr10:54782631-54782681	IMR90	lung:	fetal
46	chr10:54782631-54782681	GM12878	blood:	n/a
47	chr10:54782631-54782681	PFSK-1	brain:	n/a
48	chr10:54782631-54782681	AG09319	gingival:	n/a
49	chr10:54782631-54782681	HIPEpiC	eye:	n/a
50	chr10:54782631-54782681	SAEC	small airway:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:54767534..54770532-chr10:54779157..54781249,2	K562	blood:
2	chr10:54793499..54796412-chr10:54801093..54803641,2	MCF-7	breast:
3	chr10:54793499..54796412-chr10:54801093..54803641,2	MCF-7	breast:
4	chr10:54767534..54770532-chr10:54779157..54781249,2	K562	blood:
5	chr10:54764008..54766836-chr10:54772750..54774326,2	K562	blood:
6	chr10:54769210..54771714-chr10:54777628..54779140,2	K562	blood:
7	chr10:54764008..54766836-chr10:54772750..54774326,2	K562	blood:
8	chr10:54782310..54784916-chr10:54787401..54789318,3	MCF-7	breast:
9	chr10:54782310..54784916-chr10:54787401..54789318,3	MCF-7	breast:
10	chr10:54769210..54771714-chr10:54777628..54779140,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBL2-2	chr10:54782584-54782720	NONHSAT013446
2	lnc-MBL2-2	chr10:54789671-54789810	NONHSAT013446
3	lnc-MBL2-2	chr10:54782584-54782720	XLOC_008826
4	lnc-MBL2-2	chr10:54782584-54782720	XLOC_008826
5	lnc-MBL2-2	chr10:54789671-54789855	XLOC_008826
6	lnc-DKK1-3	chr10:54798045-54798304	NONHSAT013449
7	lnc-MBL2-2	chr10:54785024-54785887	XLOC_008826
8	lnc-MBL2-2	chr10:54789671-54789884	XLOC_008826
9	lnc-MBL2-2	chr10:54789652-54790030	XLOC_008826
10	lnc-MBL2-2	chr10:54782584-54782768	XLOC_008826

No data

Variant related genes	Relation type
SNRPEP8	TF binding region
SNRPEP8	CpG island
MYB	miRNA target sites

Extended variants
information (count: 1403 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2249003	chr10:54765608-54765609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535324709	chr10:54765613-54765614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187606649	chr10:54765672-54765673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs193069990	chr10:54765673-54765674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540786476	chr10:54765704-54765705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557870393	chr10:54765729-54765730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114031039	chr10:54765750-54765751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373957935	chr10:54765760-54765761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555765814	chr10:54765771-54765772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529614438	chr10:54765777-54765778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569148822	chr10:54765804-54765805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543312704	chr10:54765810-54765811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560001929	chr10:54765823-54765824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528717710	chr10:54765858-54765859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551660235	chr10:54765879-54765880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368185224	chr10:54765901-54765902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571758579	chr10:54765904-54765905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115028219	chr10:54765905-54765906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550571231	chr10:54765944-54765945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567277212	chr10:54765948-54765949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535383838	chr10:54765951-54765952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555208837	chr10:54765986-54765987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146780175	chr10:54766017-54766018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534849294	chr10:54766091-54766092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557667890	chr10:54766098-54766099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573830588	chr10:54766119-54766120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577710633	chr10:54766122-54766123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs543100581	chr10:54766123-54766124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372818092	chr10:54766133-54766134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184109628	chr10:54766150-54766151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148539516	chr10:54766160-54766161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542628591	chr10:54766184-54766185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560115796	chr10:54766224-54766225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545655755	chr10:54766228-54766229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142725770	chr10:54766324-54766325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs118062363	chr10:54766332-54766333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187511296	chr10:54766335-54766336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142852828	chr10:54766364-54766365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150985538	chr10:54766367-54766368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560963869	chr10:54766369-54766370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192720108	chr10:54766376-54766377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs78479740	chr10:54766433-54766434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77827169	chr10:54766437-54766438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534605832	chr10:54766443-54766444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559140250	chr10:54766449-54766450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553527731	chr10:54766470-54766471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537156999	chr10:54766492-54766493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375189919	chr10:54766549-54766550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369797938	chr10:54766550-54766551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573756762	chr10:54766575-54766576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Chronic lymphocytic leukemia	21546498	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54757200-54766400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr10:54759800-54767200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr10:54760200-54765800	Weak transcription	Stomach Mucosa	stomach
4	chr10:54761000-54766000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr10:54763400-54765800	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr10:54764400-54771200	Enhancers	HepG2	liver
7	chr10:54764800-54766000	Enhancers	GM12878-XiMat	blood
8	chr10:54764800-54767600	Enhancers	Liver	Liver
9	chr10:54765200-54782600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr10:54765400-54766200	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr10:54765600-54765800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr10:54765600-54766000	Enhancers	Fetal Thymus	thymus
13	chr10:54765600-54767600	Enhancers	Fetal Intestine Small	intestine
14	chr10:54765600-54767600	Enhancers	Fetal Kidney	kidney
15	chr10:54765800-54766000	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr10:54765800-54766000	Enhancers	Stomach Mucosa	stomach
17	chr10:54765800-54766200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr10:54765800-54767600	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr10:54766000-54766600	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr10:54766000-54766600	Weak transcription	Stomach Mucosa	stomach
21	chr10:54766000-54767600	Enhancers	Fetal Intestine Large	intestine
22	chr10:54766200-54767000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr10:54766200-54767600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr10:54766400-54767600	Enhancers	Duodenum Mucosa	Duodenum
25	chr10:54766600-54766800	Enhancers	Stomach Mucosa	stomach
26	chr10:54766600-54767600	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr10:54766800-54767000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr10:54766800-54767000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr10:54766800-54767600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr10:54766800-54770000	Weak transcription	Stomach Mucosa	stomach
31	chr10:54767200-54767400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr10:54767200-54767400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr10:54767200-54767600	Enhancers	Fetal Lung	lung
34	chr10:54767400-54769600	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr10:54767600-54768800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr10:54767600-54770000	Weak transcription	Fetal Lung	lung
37	chr10:54767600-54770200	Weak transcription	Liver	Liver
38	chr10:54767600-54782200	Weak transcription	Fetal Kidney	kidney
39	chr10:54768800-54769200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr10:54769200-54772600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr10:54769800-54770800	Enhancers	Fetal Brain Female	brain
42	chr10:54770000-54770600	Enhancers	Stomach Mucosa	stomach
43	chr10:54770000-54770800	Enhancers	Fetal Lung	lung
44	chr10:54771400-54772800	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr10:54771600-54774800	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr10:54771800-54772200	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr10:54772200-54773000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr10:54772400-54773800	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr10:54772600-54772800	Enhancers	GM12878-XiMat	blood
50	chr10:54772600-54773600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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