Variant report

Variant	nsv518207
Chromosome Location	chr18:11670845-11695676
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	chr18:11688929-11689329	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr18:11688949-11689352	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr18:11694384-11694509	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr18:11671130-11671345	GM12878	blood:	n/a	chr18:11671266-11671277
5	BCL3	chr18:11688898-11689396	A549	lung:	n/a	chr18:11689212-11689225
6	BCLAF1	chr18:11688882-11689263	GM12878	blood:	n/a	chr18:11689212-11689225
7	BHLHE40	chr18:11671083-11671265	K562	blood:	n/a	chr18:11671210-11671219 chr18:11671209-11671218 chr18:11671209-11671218 chr18:11671207-11671220
8	BHLHE40	chr18:11676932-11677259	K562	blood:	n/a	n/a
9	BHLHE40	chr18:11671112-11671366	GM12878	blood:	n/a	chr18:11671210-11671219 chr18:11671209-11671218 chr18:11671209-11671218 chr18:11671207-11671220
10	BHLHE40	chr18:11689049-11689223	GM12878	blood:	n/a	chr18:11689063-11689079 chr18:11689071-11689087
11	BRCA1	chr18:11689014-11689222	HepG2	liver:	n/a	n/a
12	BRCA1	chr18:11688994-11689271	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr18:11689017-11689205	K562	blood:	n/a	n/a
14	CBX3	chr18:11688887-11689477	HCT-116	colon:	n/a	n/a
15	CEBPB	chr18:11688981-11689299	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr18:11688849-11689294	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr18:11682111-11682191	HepG2	liver:	n/a	n/a
18	CEBPD	chr18:11689001-11689165	HepG2	liver:	n/a	n/a
19	CHD2	chr18:11689709-11689973	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr18:11688938-11689375	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr18:11688956-11689350	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr18:11689732-11689887	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr18:11689038-11689242	K562	blood:	n/a	n/a
24	CHD2	chr18:11688992-11689266	GM12878	blood:	n/a	n/a
25	CHD2	chr18:11689034-11689298	HepG2	liver:	n/a	n/a
26	CREB1	chr18:11688947-11689343	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr18:11688913-11689398	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr18:11689027-11689339	A549	lung:	n/a	n/a
29	CTBP2	chr18:11688927-11690111	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr18:11689160-11689310	GM12874	blood:	n/a	n/a
31	CTCF	chr18:11672213-11672253	K562	blood:	n/a	n/a
32	CTCF	chr18:11689104-11689172	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr18:11689040-11689274	K562	blood:	n/a	n/a
34	CTCF	chr18:11689115-11689174	Fibrobl	skin:	n/a	n/a
35	CTCF	chr18:11689135-11689143	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr18:11689063-11689203	NHEK	skin:	n/a	n/a
37	CTCF	chr18:11695112-11695162	Fibrobl	skin:	n/a	n/a
38	CTCF	chr18:11689020-11689170	Caco-2	colon:	n/a	chr18:11689031-11689044
39	CTCF	chr18:11688920-11689070	NHEK	skin:	n/a	chr18:11689031-11689044
40	CTCF	chr18:11689020-11689170	HCPEpiC	choroid plexus:	n/a	chr18:11689031-11689044
41	CUX1	chr18:11688494-11688584	GM12878	blood:	n/a	n/a
42	E2F1	chr18:11689177-11689687	Hela-S3	cervix:	n/a	chr18:11689451-11689463 chr18:11689217-11689227 chr18:11689546-11689561 chr18:11689487-11689499 chr18:11689534-11689543 chr18:11689451-11689462 chr18:11689487-11689498 chr18:11689538-11689548
43	E2F4	chr18:11688499-11688765	MCF10A-Er-Src	breast:	n/a	chr18:11688546-11688553 chr18:11688546-11688553 chr18:11688546-11688553
44	E2F4	chr18:11688969-11689595	MCF10A-Er-Src	breast:	n/a	chr18:11689451-11689463 chr18:11689217-11689227 chr18:11689546-11689561 chr18:11689487-11689499 chr18:11689534-11689543 chr18:11689538-11689548
45	E2F6	chr18:11689667-11689856	K562	blood:	n/a	n/a
46	E2F6	chr18:11689431-11689596	K562	blood:	n/a	chr18:11689451-11689463 chr18:11689546-11689561 chr18:11689487-11689499 chr18:11689534-11689543 chr18:11689538-11689548
47	E2F6	chr18:11689607-11690010	K562	blood:	n/a	n/a
48	E2F6	chr18:11689552-11690113	A549	lung:	n/a	chr18:11690080-11690089 chr18:11690084-11690093
49	E2F6	chr18:11689026-11690136	H1-hESC	embryonic stem cell:	n/a	chr18:11690080-11690089 chr18:11689451-11689463 chr18:11689217-11689227 chr18:11689546-11689561 chr18:11689487-11689499 chr18:11689534-11689543 chr18:11690084-11690093 chr18:11689538-11689548
50	E2F6	chr18:11688898-11690144	H1-hESC	embryonic stem cell:	n/a	chr18:11690080-11690089 chr18:11689451-11689463 chr18:11689217-11689227 chr18:11689546-11689561 chr18:11689487-11689499 chr18:11689534-11689543 chr18:11690084-11690093 chr18:11689538-11689548

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:11689206-11689256	HPAEpiC	pulmonary alveolar:	n/a
2	chr18:11685789-11685839	HepG2	liver:	n/a
3	chr18:11689206-11689256	ovcar-3	ovarian:	n/a
4	chr18:11689613-11689663	NH-A	brain:	n/a
5	chr18:11690145-11690195	BJ	skin:	n/a
6	chr18:11688972-11689022	PrEC	prostate:	n/a
7	chr18:11689062-11689112	HNPCEpiC	eye:	n/a
8	chr18:11690145-11690195	HRCEpiC	kidney:	n/a
9	chr18:11689032-11689082	MCF-7	breast:	n/a
10	chr18:11688011-11688061	CMK	blood:	n/a
11	chr18:11689024-11689074	HNPCEpiC	eye:	n/a
12	chr18:11688972-11689022	SK-N-SH_RA	brain:	n/a
13	chr18:11685789-11685839	HL-60	blood:	n/a
14	chr18:11689062-11689112	GM12891	blood:	n/a
15	chr18:11685789-11685839	HCM	heart:	n/a
16	chr18:11689032-11689082	AoSMC	blood vessel:	n/a
17	chr18:11688011-11688061	NB4	blood:	n/a
18	chr18:11689218-11689268	PANC-1	pancreas:	n/a
19	chr18:11688988-11689038	AG10803	skin:	n/a
20	chr18:11688972-11689022	AG10803	skin:	n/a
21	chr18:11688011-11688061	HL-60	blood:	n/a
22	chr18:11688008-11688058	HEEpiC	esophagus:	n/a
23	chr18:11692420-11692470	AG10803	skin:	n/a
24	chr18:11689613-11689663	HRPEpiC	eye:	n/a
25	chr18:11688972-11689022	CMK	blood:	n/a
26	chr18:11690145-11690195	GM12892	blood:	n/a
27	chr18:11688011-11688061	T-47D	breast:	n/a
28	chr18:11689032-11689082	HRE	kidney:	n/a
29	chr18:11689284-11689334	SK-N-SH	brain:	n/a
30	chr18:11688011-11688061	NHBE	bronchial:	n/a
31	chr18:11688011-11688061	SK-N-SH	brain:	n/a
32	chr18:11688011-11688061	PrEC	prostate:	n/a
33	chr18:11688972-11689022	HRPEpiC	eye:	n/a
34	chr18:11689024-11689074	AoSMC	blood vessel:	n/a
35	chr18:11692420-11692470	HCPEpiC	choroid plexus:	n/a
36	chr18:11689062-11689112	ECC-1	luminal epithelium:	n/a
37	chr18:11689284-11689334	AG04450	lung:	fetal
38	chr18:11688011-11688061	HMEC	breast:	n/a
39	chr18:11688772-11688822	LNCaP	prostate:	n/a
40	chr18:11690145-11690195	MCF10A-Er-Src	breast:	n/a
41	chr18:11688008-11688058	HRCEpiC	kidney:	n/a
42	chr18:11688988-11689038	HepG2	liver:	n/a
43	chr18:11688008-11688058	NHBE	bronchial:	n/a
44	chr18:11688988-11689038	SK-N-SH_RA	brain:	n/a
45	chr18:11688988-11689038	Hela-S3	cervix:	n/a
46	chr18:11688972-11689022	ProgFib	skin:	n/a
47	chr18:11689284-11689334	ovcar-3	ovarian:	n/a
48	chr18:11688972-11689022	ECC-1	luminal epithelium:	n/a
49	chr18:11688972-11689022	GM12878	blood:	n/a
50	chr18:11689284-11689334	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:11675703..11677385-chr18:11679349..11680961,2	K562	blood:
2	chr18:11675703..11677385-chr18:11679349..11680961,2	K562	blood:
3	chr18:11661437..11663649-chr18:11686391..11688864,2	K562	blood:
4	chr18:11662625..11665139-chr18:11684651..11687441,2	MCF-7	breast:
5	chr18:11665029..11667238-chr18:11692110..11694200,2	K562	blood:

Variant related genes	Relation type
GNAL	TF binding region
ENSG00000260759	TF binding region
GNAL	CpG island
ENSG00000260759	CpG island

Extended variants
information (count: 1011 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1011 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12961855	chr18:11670845-11670846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114905608	chr18:11670867-11670868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs578111871	chr18:11670913-11670914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12962341	chr18:11670927-11670928	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs12962122	chr18:11670976-11670977	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs546251007	chr18:11670994-11670995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375279958	chr18:11671041-11671042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565224347	chr18:11671049-11671050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532259540	chr18:11671050-11671051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551393275	chr18:11671075-11671076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560137764	chr18:11671076-11671077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192409496	chr18:11671142-11671143	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs114938676	chr18:11671158-11671159	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs28479287	chr18:11671164-11671165	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs531892423	chr18:11671167-11671168	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs538476311	chr18:11671208-11671209	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs28485115	chr18:11671214-11671215	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs12966339	chr18:11671231-11671232	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs12967201	chr18:11671239-11671240	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs554475559	chr18:11671291-11671292	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs113878256	chr18:11671302-11671303	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs572086212	chr18:11671303-11671304	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs184750980	chr18:11671338-11671339	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs12966486	chr18:11671340-11671341	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs576047184	chr18:11671347-11671348	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs543636692	chr18:11671392-11671393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140405352	chr18:11671406-11671407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541100664	chr18:11671431-11671432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs9953163	chr18:11671492-11671493	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs374525225	chr18:11671495-11671496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540944618	chr18:11671496-11671497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566432846	chr18:11671497-11671498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377694234	chr18:11671520-11671521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs58780734	chr18:11671536-11671537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549104078	chr18:11671551-11671552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561470390	chr18:11671557-11671558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79128720	chr18:11671591-11671592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550377942	chr18:11671597-11671598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571891654	chr18:11671598-11671599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533571216	chr18:11671599-11671600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539200799	chr18:11671648-11671649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs56814182	chr18:11671658-11671659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs59573562	chr18:11671659-11671660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28460484	chr18:11671706-11671707	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs540498384	chr18:11671748-11671749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74177573	chr18:11671757-11671758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2186961	chr18:11671759-11671760	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs554252936	chr18:11671773-11671774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35094433	chr18:11671798-11671799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569761321	chr18:11671822-11671823	Weak transcription	n/a	n/a	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
abnormal development	18461090	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:372 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11669600-11675000	Weak transcription	Right Atrium	heart
2	chr18:11670200-11677000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr18:11670600-11671000	Weak transcription	Esophagus	oesophagus
4	chr18:11671000-11671200	Enhancers	Esophagus	oesophagus
5	chr18:11671200-11677000	Weak transcription	Esophagus	oesophagus
6	chr18:11673600-11673800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr18:11676800-11677200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr18:11677000-11677200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr18:11677000-11677200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr18:11677000-11677200	Bivalent/Poised TSS	Liver	Liver
11	chr18:11677000-11677200	Enhancers	Esophagus	oesophagus
12	chr18:11677000-11677200	Enhancers	Spleen	Spleen
13	chr18:11677000-11677200	Flanking Bivalent TSS/Enh	A549	lung
14	chr18:11677200-11688400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr18:11678000-11678200	Flanking Active TSS	Fetal Brain Male	brain
16	chr18:11678200-11678800	Enhancers	Fetal Brain Male	brain
17	chr18:11678200-11679200	Enhancers	Fetal Brain Female	brain
18	chr18:11688200-11688400	Enhancers	Hela-S3	cervix
19	chr18:11688400-11688600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
20	chr18:11688400-11688600	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr18:11688400-11688600	Enhancers	Brain Hippocampus Middle	brain
22	chr18:11688400-11688600	Enhancers	Colon Smooth Muscle	Colon
23	chr18:11688400-11688600	Enhancers	Stomach Smooth Muscle	stomach
24	chr18:11688400-11688800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
25	chr18:11688400-11688800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr18:11688400-11688800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr18:11688400-11689000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr18:11688400-11689000	Flanking Active TSS	Hela-S3	cervix
29	chr18:11688400-11689400	Active TSS	Fetal Brain Female	brain
30	chr18:11688600-11688800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr18:11688600-11688800	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
32	chr18:11688600-11688800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
33	chr18:11688600-11688800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr18:11688600-11688800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr18:11688600-11688800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr18:11688600-11688800	Bivalent Enhancer	Liver	Liver
37	chr18:11688600-11688800	Enhancers	Brain Anterior Caudate	brain
38	chr18:11688600-11688800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
39	chr18:11688600-11688800	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
40	chr18:11688600-11688800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
41	chr18:11688600-11688800	Bivalent Enhancer	Fetal Heart	heart
42	chr18:11688600-11688800	Bivalent Enhancer	Fetal Kidney	kidney
43	chr18:11688600-11688800	Bivalent Enhancer	Fetal Muscle Leg	muscle
44	chr18:11688600-11688800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
45	chr18:11688600-11688800	Enhancers	NHEK	skin
46	chr18:11688600-11689000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr18:11688600-11689000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
48	chr18:11688600-11689000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
49	chr18:11688600-11689000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
50	chr18:11688600-11689000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast

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