Variant report

Variant	nsv909397
Chromosome Location	chr18:12062004-12083314
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:314)
CpG islands
(count:733)
Chromatin interactive
region (count:5)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr18:12076645-12076788	K562	blood:	n/a	n/a
2	CEBPB	chr18:12069020-12069213	IMR90	lung:	n/a	n/a
3	CEBPB	chr18:12069057-12069324	K562	blood:	n/a	n/a
4	CEBPB	chr18:12067926-12068149	K562	blood:	n/a	n/a
5	CEBPB	chr18:12067920-12068124	HepG2	liver:	n/a	n/a
6	CREB1	chr18:12076434-12076834	A549	lung:	n/a	n/a
7	CTCF	chr18:12074860-12075010	HFF	foreskin:	n/a	n/a
8	CTCF	chr18:12068500-12068650	HCFaa	heart:	n/a	n/a
9	CTCF	chr18:12074860-12075010	HEK293	kidney:	n/a	n/a
10	CTCF	chr18:12074840-12074990	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr18:12074868-12074952	ProgFib	skin:	n/a	n/a
12	CTCF	chr18:12068476-12068627	Pancreas_OC	pancreas:	n/a	n/a
13	CTCF	chr18:12074793-12074998	K562	blood:	n/a	n/a
14	CTCF	chr18:12064578-12064639	ProgFib	skin:	n/a	n/a
15	CTCF	chr18:12074880-12074950	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr18:12074840-12074990	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr18:12068422-12068749	K562	blood:	n/a	n/a
18	CTCF	chr18:12074860-12075010	GM12869	blood:	n/a	n/a
19	CTCF	chr18:12074888-12074967	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr18:12074840-12074990	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr18:12068365-12068712	K562	blood:	n/a	n/a
22	CTCF	chr18:12074840-12074990	HA-sp	spinal cord:	n/a	n/a
23	CTCF	chr18:12068507-12068611	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr18:12068520-12068670	GM12864	blood:	n/a	n/a
25	CTCF	chr18:12074852-12075015	GM19239	blood:	n/a	n/a
26	CTCF	chr18:12068437-12068606	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr18:12074780-12074930	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr18:12068460-12068610	K562	blood:	n/a	n/a
29	CTCF	chr18:12074840-12074990	HAc	cerebellar:	n/a	n/a
30	CTCF	chr18:12074847-12075002	GM12892	blood:	n/a	n/a
31	CTCF	chr18:12074754-12075101	GM12878	blood:	n/a	n/a
32	CTCF	chr18:12074858-12074993	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr18:12068419-12068723	IMR90	lung:	n/a	n/a
34	CTCF	chr18:12074860-12075010	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr18:12074852-12074996	Gliobla	brain:	n/a	n/a
36	CTCF	chr18:12074860-12075010	SAEC	small airway:	n/a	n/a
37	CTCF	chr18:12074841-12075002	K562	blood:	n/a	n/a
38	CTCF	chr18:12074880-12075030	GM12875	blood:	n/a	n/a
39	CTCF	chr18:12074860-12075010	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr18:12074814-12075038	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr18:12074900-12075050	BJ	skin:	n/a	n/a
42	CTCF	chr18:12068470-12068583	GM20000	blood:	n/a	n/a
43	CTCF	chr18:12074800-12074950	K562	blood:	n/a	n/a
44	CTCF	chr18:12068460-12068610	GM12871	blood:	n/a	n/a
45	CTCF	chr18:12074820-12074970	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr18:12068460-12068610	GM12864	blood:	n/a	n/a
47	CTCF	chr18:12074840-12074990	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr18:12068540-12068690	GM12865	blood:	n/a	n/a
49	CTCF	chr18:12068261-12068747	K562	blood:	n/a	n/a
50	CTCF	chr18:12074920-12075070	HCM	heart:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12068363-12068413	GM12892	blood:	n/a
2	chr18:12068363-12068413	GM12892	blood:	n/a
3	chr18:12073455-12073505	RPTEC	kidney:	n/a
4	chr18:12076365-12076415	NH-A	brain:	n/a
5	chr18:12072395-12072445	Hela-S3	cervix:	n/a
6	chr18:12068099-12068149	Jurkat	blood:	n/a
7	chr18:12068099-12068149	Hela-S3	cervix:	n/a
8	chr18:12068363-12068413	T-47D	breast:	n/a
9	chr18:12068065-12068115	PANC-1	pancreas:	n/a
10	chr18:12068065-12068115	T-47D	breast:	n/a
11	chr18:12076365-12076415	AG04449	skin:	fetal
12	chr18:12068065-12068115	SK-N-SH	brain:	n/a
13	chr18:12068363-12068413	AG09319	gingival:	n/a
14	chr18:12068099-12068149	HMEC	breast:	n/a
15	chr18:12073455-12073505	HRPEpiC	eye:	n/a
16	chr18:12068099-12068149	PANC-1	pancreas:	n/a
17	chr18:12072395-12072445	IMR90	lung:	fetal
18	chr18:12077147-12077197	H1-hESC	embryonic stem cell:	embryo
19	chr18:12076365-12076415	HNPCEpiC	eye:	n/a
20	chr18:12076435-12076485	HCPEpiC	choroid plexus:	n/a
21	chr18:12073455-12073505	PANC-1	pancreas:	n/a
22	chr18:12068363-12068413	SAEC	small airway:	n/a
23	chr18:12073455-12073505	PFSK-1	brain:	n/a
24	chr18:12073455-12073505	NB4	blood:	n/a
25	chr18:12072395-12072445	HMEC	breast:	n/a
26	chr18:12068099-12068149	HepG2	liver:	n/a
27	chr18:12073455-12073505	HCT-116	colon:	n/a
28	chr18:12068884-12068934	Jurkat	blood:	n/a
29	chr18:12076476-12076526	GM12891	blood:	n/a
30	chr18:12076435-12076485	BE2_C	brain:	n/a
31	chr18:12068363-12068413	K562	blood:	n/a
32	chr18:12068065-12068115	ProgFib	skin:	n/a
33	chr18:12064388-12064438	HAEpiC	amniotic membrane:	n/a
34	chr18:12072395-12072445	A549	lung:	n/a
35	chr18:12068884-12068934	BE2_C	brain:	n/a
36	chr18:12064388-12064438	AG04450	lung:	fetal
37	chr18:12076435-12076485	GM12892	blood:	n/a
38	chr18:12073455-12073505	HAEpiC	amniotic membrane:	n/a
39	chr18:12073455-12073505	Caco-2	colon:	n/a
40	chr18:12064388-12064438	LNCaP	prostate:	n/a
41	chr18:12068363-12068413	AoSMC	blood vessel:	n/a
42	chr18:12076435-12076485	HPAEpiC	pulmonary alveolar:	n/a
43	chr18:12076365-12076415	ProgFib	skin:	n/a
44	chr18:12064388-12064438	PANC-1	pancreas:	n/a
45	chr18:12076476-12076526	GM12878	blood:	n/a
46	chr18:12076476-12076526	AG09319	gingival:	n/a
47	chr18:12076435-12076485	HRE	kidney:	n/a
48	chr18:12072395-12072445	HRE	kidney:	n/a
49	chr18:12068065-12068115	AG09309	skin:	n/a
50	chr18:12068099-12068149	ECC-1	luminal epithelium:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:12063010..12065990-chr19:13351067..13352603,2	MCF-7	breast:
2	chr18:12057151..12059400-chr18:12062481..12064510,2	K562	blood:
3	chr18:12067124..12068644-chr19:18543710..18545856,2	K562	blood:
4	chr18:12067124..12068647-chr19:18543710..18545740,2	K562	blood:
5	chr18:12076450..12076959-chr4:22517248..22517778,2	HCT-116	colon:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD62-2	chr18:12081796-12081838	ENSG00000267722.1
2	lnc-ANKRD62-1	chr18:12074792-12075074	XLOC_012628
3	lnc-ANKRD62-1	chr18:12073319-12073537	XLOC_012628
4	lnc-ANKRD62-2	chr18:12081539-12081657	ENSG00000267722.1

No data

Variant related genes	Relation type
ENSG00000212712	TF binding region
ENSG00000267722	TF binding region
ENSG00000256616	TF binding region
ENSG00000267533	TF binding region
ENSG00000212712	CpG island
ENSG00000267722	CpG island
ENSG00000256616	CpG island
ENSG00000267533	CpG island
ENSG00000130511	chromatin interactions
ENSG00000212712	chromatin interactions
ENSG00000152990	chromatin interactions

Extended variants
information (count: 898 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:898 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56161891	chr18:12062004-12062005	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs531664790	chr18:12062030-12062031	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs144537730	chr18:12062050-12062051	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs34339997	chr18:12062074-12062075	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs571388962	chr18:12062084-12062085	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs36061429	chr18:12062091-12062092	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs150341800	chr18:12062108-12062109	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs184151421	chr18:12062114-12062115	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs112710442	chr18:12062117-12062118	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs138065694	chr18:12062118-12062119	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs60505533	chr18:12062119-12062120	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs148543184	chr18:12062124-12062125	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs566626542	chr18:12062148-12062149	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs538731439	chr18:12062195-12062196	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs367779612	chr18:12062199-12062200	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs145075157	chr18:12062242-12062243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79345699	chr18:12062254-12062255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs58185239	chr18:12062255-12062256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78692826	chr18:12062257-12062258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371996669	chr18:12062319-12062320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs28535741	chr18:12062334-12062335	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs188748745	chr18:12062336-12062337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373874327	chr18:12062360-12062361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534893351	chr18:12062364-12062365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556600701	chr18:12062365-12062366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs578099844	chr18:12062366-12062367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528290716	chr18:12062367-12062368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545284496	chr18:12062368-12062369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs68021189	chr18:12062369-12062370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575789939	chr18:12062375-12062376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181574271	chr18:12062416-12062417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553858559	chr18:12062422-12062423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536395803	chr18:12062423-12062424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542628566	chr18:12062431-12062432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560893538	chr18:12062453-12062454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555152535	chr18:12062459-12062460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531226588	chr18:12062476-12062477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186127622	chr18:12062477-12062478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565041513	chr18:12062485-12062486	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs113349329	chr18:12062553-12062554	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs28567958	chr18:12062582-12062583	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs34222301	chr18:12062597-12062598	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs547235072	chr18:12062603-12062604	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs566618384	chr18:12062623-12062624	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs527815898	chr18:12062672-12062673	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs540957491	chr18:12062691-12062692	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs567622573	chr18:12062703-12062704	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537871214	chr18:12062724-12062725	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs190479288	chr18:12062732-12062733	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs550410996	chr18:12062742-12062743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12054200-12063400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr18:12055600-12076400	Weak transcription	Right Atrium	heart
3	chr18:12060800-12064400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr18:12061000-12062200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr18:12062000-12064400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr18:12062000-12064400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr18:12062200-12064400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr18:12063000-12063200	Enhancers	Right Ventricle	heart
9	chr18:12063600-12064000	Enhancers	Fetal Muscle Trunk	muscle
10	chr18:12064400-12064600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr18:12064400-12064600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
12	chr18:12064400-12064800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr18:12064400-12064800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr18:12064400-12064800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr18:12064600-12064800	Active TSS	Breast Myoepithelial Primary Cells	Breast
16	chr18:12064600-12067000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr18:12064800-12065000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr18:12064800-12065400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr18:12065800-12066000	Enhancers	H9 Cell Line	embryonic stem cell
20	chr18:12066000-12076400	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr18:12067000-12068600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr18:12067400-12068400	Enhancers	Fetal Muscle Trunk	muscle
23	chr18:12068000-12068600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr18:12068200-12068600	Active TSS	Pancreas	Pancrea
25	chr18:12068200-12068800	Active TSS	HUVEC	blood vessel
26	chr18:12068200-12069000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr18:12068600-12069200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr18:12068600-12076400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr18:12068800-12069000	Bivalent/Poised TSS	Osteobl	bone
30	chr18:12068800-12069200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr18:12068800-12069200	Enhancers	Fetal Lung	lung
32	chr18:12068800-12069200	Flanking Active TSS	HUVEC	blood vessel
33	chr18:12069000-12069200	Active TSS	Osteobl	bone
34	chr18:12069200-12069400	Enhancers	HUVEC	blood vessel
35	chr18:12069200-12071000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr18:12069400-12070600	Weak transcription	HUVEC	blood vessel
37	chr18:12070600-12072200	Enhancers	HUVEC	blood vessel
38	chr18:12071000-12071400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr18:12072200-12076400	Weak transcription	HUVEC	blood vessel
40	chr18:12074600-12077000	Active TSS	Fetal Brain Female	brain
41	chr18:12075000-12075400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr18:12075400-12076600	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr18:12076000-12076200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
44	chr18:12076200-12076400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
45	chr18:12076200-12076400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
46	chr18:12076200-12076400	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr18:12076200-12076400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr18:12076200-12076400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
49	chr18:12076200-12076400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
50	chr18:12076200-12076400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell

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