Variant report

Variant	nsv833641
Chromosome Location	chr18:44815063-45020202
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	ATF2	chr18:44948988-44949313	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr18:44944214-44944544	GM12878	blood:	n/a	n/a
3	ATF3	chr18:44948910-44949254	K562	blood:	n/a	n/a
4	BACH1	chr18:44962373-44962705	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr18:44914269-44914590	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr18:44914275-44914557	K562	blood:	n/a	n/a
7	BATF	chr18:44944138-44944558	GM12878	blood:	n/a	chr18:44944313-44944324 chr18:44944314-44944324
8	BATF	chr18:44944225-44944521	GM12878	blood:	n/a	chr18:44944313-44944324 chr18:44944314-44944324
9	BCL3	chr18:44944252-44944646	GM12878	blood:	n/a	n/a
10	BHLHE40	chr18:44946649-44946846	GM12878	blood:	n/a	n/a
11	BHLHE40	chr18:44934931-44934940	K562	blood:	n/a	n/a
12	BHLHE40	chr18:44847002-44847019	K562	blood:	n/a	n/a
13	BRCA1	chr18:44924131-44924343	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr18:44988430-44988698	H1-hESC	embryonic stem cell:	n/a	chr18:44988522-44988535
15	CEBPB	chr18:44961513-44961702	H1-hESC	embryonic stem cell:	n/a	chr18:44961673-44961686 chr18:44961675-44961686 chr18:44961610-44961621
16	CEBPB	chr18:44961509-44961709	K562	blood:	n/a	chr18:44961673-44961686 chr18:44961675-44961686 chr18:44961610-44961621
17	CEBPB	chr18:44996397-44996675	IMR90	lung:	n/a	n/a
18	CEBPB	chr18:44868461-44868561	HepG2	liver:	n/a	chr18:44868530-44868541 chr18:44868530-44868541 chr18:44868531-44868542 chr18:44868495-44868503
19	CEBPB	chr18:44861409-44861698	HepG2	liver:	n/a	chr18:44861548-44861561 chr18:44861549-44861560 chr18:44861686-44861694
20	CEBPB	chr18:44961501-44961780	A549	lung:	n/a	chr18:44961673-44961686 chr18:44961675-44961686 chr18:44961610-44961621
21	CEBPB	chr18:44870242-44870442	H1-hESC	embryonic stem cell:	n/a	chr18:44870362-44870375 chr18:44870362-44870373
22	CEBPB	chr18:44923836-44923913	HepG2	liver:	n/a	n/a
23	CEBPB	chr18:44870245-44870531	IMR90	lung:	n/a	chr18:44870362-44870375 chr18:44870362-44870373
24	CEBPB	chr18:44870193-44870518	HepG2	liver:	n/a	chr18:44870362-44870375 chr18:44870362-44870373
25	CEBPB	chr18:44961467-44961797	HepG2	liver:	n/a	chr18:44961673-44961686 chr18:44961675-44961686 chr18:44961610-44961621
26	CEBPB	chr18:44979413-44979710	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr18:44870224-44870527	A549	lung:	n/a	chr18:44870362-44870375 chr18:44870362-44870373
28	CEBPB	chr18:44999916-44999946	A549	lung:	n/a	n/a
29	CEBPB	chr18:44948963-44949290	K562	blood:	n/a	n/a
30	CEBPB	chr18:44961499-44961803	IMR90	lung:	n/a	chr18:44961673-44961686 chr18:44961675-44961686 chr18:44961610-44961621
31	CEBPB	chr18:44949019-44949262	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr18:44979441-44979726	A549	lung:	n/a	n/a
33	CEBPB	chr18:44849793-44849985	HepG2	liver:	n/a	n/a
34	CEBPB	chr18:44996535-44996607	K562	blood:	n/a	n/a
35	CEBPB	chr18:44898113-44898290	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr18:44967901-44968083	HepG2	liver:	n/a	n/a
37	CEBPB	chr18:44870198-44870519	Hela-S3	cervix:	n/a	chr18:44870362-44870375 chr18:44870362-44870373
38	CEBPB	chr18:44979399-44979728	IMR90	lung:	n/a	n/a
39	CEBPB	chr18:44870237-44870463	K562	blood:	n/a	chr18:44870362-44870375 chr18:44870362-44870373
40	CEBPB	chr18:44924270-44924407	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr18:44979414-44979751	HepG2	liver:	n/a	n/a
42	CHD2	chr18:44946602-44946952	GM12878	blood:	n/a	n/a
43	CTCF	chr18:44871820-44871970	WERI-Rb-1	eye:	n/a	chr18:44871901-44871919 chr18:44871903-44871924
44	CTCF	chr18:44924160-44924310	SK-N-SH_RA	brain:	n/a	chr18:44924238-44924259 chr18:44924236-44924254 chr18:44924237-44924253
45	CTCF	chr18:44924117-44924587	H1-hESC	embryonic stem cell:	n/a	chr18:44924238-44924259 chr18:44924236-44924254 chr18:44924237-44924253
46	CTCF	chr18:44833688-44833800	Gliobla	brain:	n/a	n/a
47	CTCF	chr18:44949000-44949150	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr18:44871886-44871920	GM12892	blood:	n/a	chr18:44871901-44871919
49	CTCF	chr18:44871840-44871990	WERI-Rb-1	eye:	n/a	chr18:44871901-44871919 chr18:44871903-44871924
50	CTCF	chr18:44924160-44924310	HepG2	liver:	n/a	chr18:44924238-44924259 chr18:44924236-44924254 chr18:44924237-44924253

No.	Distal block	Cell Line	Cell type
1	chr18:44810240..44811750-chr18:44815375..44817076,2	K562	blood:
2	chr18:44842533..44845221-chr18:44847289..44849920,2	K562	blood:
3	chr18:44944185..44945967-chr18:44952003..44954694,2	MCF-7	breast:
4	chr18:44811639..44814286-chr18:44814961..44816787,2	MCF-7	breast:
5	chr18:44938043..44940692-chr18:44942276..44945492,3	K562	blood:
6	chr18:44938043..44940692-chr18:44942276..44945492,3	K562	blood:
7	chr18:44974280..44977864-chr18:44980316..44983533,3	K562	blood:
8	chr18:44944185..44945967-chr18:44952003..44954694,2	MCF-7	breast:
9	chr18:44923783..44924527-chr18:45275630..45276152,2	K562	blood:
10	chr18:44842533..44845221-chr18:44847289..44849920,2	K562	blood:
11	chr18:44974280..44977864-chr18:44980316..44983533,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KATNAL2-8	chr18:44828496-44828841	ucscGeneNc_uc002ldh_1
2	lnc-KATNAL2-9	chr18:44831747-44831786	NONHSAT059161
3	lnc-KATNAL2-8	chr18:44820368-44820437	ucscGeneNc_uc002ldh_1
4	lnc-KATNAL2-9	chr18:44832266-44832435	NONHSAT059161

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4527	chr18:44906874-44906895	MIMAT0019066

Variant related genes	Relation type
MIR4527	TF binding region
ENSG00000267761	chromatin interactions

Extended variants
information (count: 4606 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4606 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34864037	chr18:44815105-44815106	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs16950744	chr18:44815110-44815111	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs2850693	chr18:44815122-44815123	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs532520733	chr18:44815134-44815135	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs1347341	chr18:44815221-44815222	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs566026502	chr18:44815225-44815226	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs535262665	chr18:44815240-44815241	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs555199978	chr18:44815242-44815243	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs5824659	chr18:44815262-44815263	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs568813468	chr18:44815263-44815264	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs189619787	chr18:44815284-44815285	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556194571	chr18:44815311-44815312	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs1434505	chr18:44815330-44815331	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs1347340	chr18:44815363-44815364	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs28417368	chr18:44815401-44815402	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs180898877	chr18:44815408-44815409	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs79550416	chr18:44815418-44815419	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs397949882	chr18:44815420-44815421	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs540875156	chr18:44815424-44815425	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs190950688	chr18:44815438-44815439	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs369499086	chr18:44815496-44815497	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181827668	chr18:44815531-44815532	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs563547674	chr18:44815536-44815537	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532571949	chr18:44815544-44815545	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552265402	chr18:44815545-44815546	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559785547	chr18:44815563-44815564	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs1347339	chr18:44815566-44815567	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs376190283	chr18:44815570-44815571	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548807319	chr18:44815621-44815622	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs568620290	chr18:44815650-44815651	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs537766511	chr18:44815664-44815665	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs185975444	chr18:44815703-44815704	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs34424939	chr18:44815729-44815730	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs546957780	chr18:44815746-44815747	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs540693562	chr18:44815760-44815761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs564075578	chr18:44815813-44815814	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs116017984	chr18:44815821-44815822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs16950754	chr18:44815854-44815855	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs558265626	chr18:44815873-44815874	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs190485301	chr18:44815911-44815912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs139164745	chr18:44815936-44815937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs539378619	chr18:44815980-44815981	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs554345764	chr18:44816030-44816031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs183422356	chr18:44816069-44816070	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114002352	chr18:44816138-44816139	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs77529588	chr18:44816218-44816219	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs188006372	chr18:44816229-44816230	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs77677293	chr18:44816237-44816238	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs191231845	chr18:44816259-44816260	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs16950767	chr18:44816274-44816275	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	21569311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44810400-44819200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr18:44813400-44815400	Weak transcription	Pancreas	Pancrea
3	chr18:44814200-44815200	Enhancers	Brain Cingulate Gyrus	brain
4	chr18:44814200-44815600	Bivalent Enhancer	Brain Germinal Matrix	brain
5	chr18:44814400-44815200	Bivalent Enhancer	Fetal Brain Female	brain
6	chr18:44814800-44815200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr18:44814800-44815200	Bivalent Enhancer	Fetal Brain Male	brain
8	chr18:44814800-44815400	Enhancers	Brain Hippocampus Middle	brain
9	chr18:44815000-44815200	Enhancers	HepG2	liver
10	chr18:44815400-44816200	Enhancers	Pancreas	Pancrea
11	chr18:44817400-44817600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
12	chr18:44819200-44819400	Enhancers	Muscle Satellite Cultured Cells	--
13	chr18:44833400-44833600	Bivalent Enhancer	Brain Germinal Matrix	brain
14	chr18:44837400-44837600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr18:44839800-44840600	Enhancers	Brain Cingulate Gyrus	brain
16	chr18:44839800-44858400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr18:44840000-44840800	Enhancers	Brain Hippocampus Middle	brain
18	chr18:44840000-44841000	Enhancers	Brain Substantia Nigra	brain
19	chr18:44840200-44840600	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr18:44840200-44840800	Enhancers	Muscle Satellite Cultured Cells	--
21	chr18:44840600-44840800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr18:44840800-44841200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr18:44840800-44841200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
24	chr18:44840800-44849400	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr18:44849400-44850000	Enhancers	Muscle Satellite Cultured Cells	--
26	chr18:44854000-44854400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr18:44854000-44854800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr18:44854000-44855000	Enhancers	H9 Cell Line	embryonic stem cell
29	chr18:44854400-44855000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr18:44854400-44855000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr18:44854400-44855000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr18:44854600-44855000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr18:44856400-44856600	Bivalent Enhancer	Brain Germinal Matrix	brain
34	chr18:44857200-44858200	Enhancers	NHDF-Ad	bronchial
35	chr18:44857400-44858600	Bivalent Enhancer	Brain Germinal Matrix	brain
36	chr18:44858200-44858800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr18:44858400-44858600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr18:44858600-44860000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr18:44859800-44862200	Enhancers	Brain Germinal Matrix	brain
40	chr18:44860200-44860400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr18:44860400-44861000	Enhancers	Fetal Brain Female	brain
42	chr18:44863800-44864200	Enhancers	Spleen	Spleen
43	chr18:44868800-44870800	Enhancers	HSMM	muscle
44	chr18:44868800-44872000	Enhancers	Muscle Satellite Cultured Cells	--
45	chr18:44869200-44869600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr18:44869200-44870400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr18:44869200-44872400	Enhancers	NHDF-Ad	bronchial
48	chr18:44870000-44870400	Enhancers	NH-A	brain
49	chr18:44871800-44872800	Enhancers	Pancreas	Pancrea
50	chr18:44871800-44873600	Enhancers	Brain Germinal Matrix	brain

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