Variant report

Variant	esv1821757
Chromosome Location	chr18:43910908-43914085
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	BACH1	chr18:43912950-43914058	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr18:43913455-43913716	HepG2	liver:	n/a	n/a
3	BHLHE40	chr18:43913571-43913771	GM12878	blood:	n/a	n/a
4	BRCA1	chr18:43912864-43912905	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr18:43911341-43911698	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr18:43911342-43911682	HepG2	liver:	n/a	n/a
7	CEBPB	chr18:43911467-43911616	K562	blood:	n/a	n/a
8	CEBPB	chr18:43913479-43914028	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr18:43913251-43914211	Hela-S3	cervix:	n/a	chr18:43913992-43913999 chr18:43914023-43914030
10	CTCF	chr18:43913672-43913681	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr18:43913660-43913810	SK-N-SH_RA	brain:	n/a	n/a
12	CTCF	chr18:43913686-43913691	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr18:43913320-43913470	GM12866	blood:	n/a	n/a
14	CTCF	chr18:43913000-43913150	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr18:43913064-43913123	MCF-7	breast:	n/a	n/a
16	CTCF	chr18:43913640-43913790	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr18:43913500-43913650	SAEC	small airway:	n/a	n/a
18	CTCF	chr18:43913540-43913690	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr18:43913638-43913757	NHEK	skin:	n/a	n/a
20	CTCF	chr18:43913083-43913130	MCF-7	breast:	n/a	n/a
21	CTCF	chr18:43913644-43913730	MCF-7	breast:	n/a	n/a
22	CTCF	chr18:43913668-43913747	MCF-7	breast:	n/a	n/a
23	CTCF	chr18:43913720-43913870	SAEC	small airway:	n/a	n/a
24	CTCF	chr18:43913695-43913743	MCF-7	breast:	n/a	n/a
25	CTCF	chr18:43913707-43913711	A549	lung:	n/a	n/a
26	CTCF	chr18:43913744-43913746	MCF-7	breast:	n/a	n/a
27	E2F1	chr18:43913480-43914374	Hela-S3	cervix:	n/a	chr18:43913835-43913846 chr18:43913992-43913999 chr18:43913861-43913870 chr18:43913760-43913774 chr18:43913987-43914001 chr18:43914023-43914030
28	ELK1	chr18:43913599-43914036	Hela-S3	cervix:	n/a	n/a
29	GABPA	chr18:43913389-43913704	H1-hESC	embryonic stem cell:	n/a	n/a
30	GTF2F1	chr18:43913117-43914067	Hela-S3	cervix:	n/a	n/a
31	GTF2F1	chr18:43910907-43910984	H1-hESC	embryonic stem cell:	n/a	n/a
32	GTF2F1	chr18:43913448-43913652	H1-hESC	embryonic stem cell:	n/a	n/a
33	HA-E2F1	chr18:43912907-43914083	MCF-7	breast:	n/a	chr18:43913835-43913846 chr18:43913992-43913999 chr18:43913861-43913870 chr18:43913760-43913774 chr18:43913987-43914001 chr18:43914023-43914030
34	HA-E2F1	chr18:43913510-43914412	Hela-S3	cervix:	n/a	chr18:43913835-43913846 chr18:43913992-43913999 chr18:43913861-43913870 chr18:43913760-43913774 chr18:43913987-43914001 chr18:43914023-43914030
35	KAP1	chr18:43912996-43913731	HEK293	kidney:	n/a	n/a
36	MAFK	chr18:43913358-43913825	Hela-S3	cervix:	n/a	n/a
37	MAX	chr18:43912884-43913952	MCF-7	breast:	n/a	chr18:43912943-43912952 chr18:43913176-43913186
38	MAX	chr18:43913071-43914131	HCT-116	colon:	n/a	chr18:43913176-43913186
39	MAX	chr18:43912842-43914127	H1-hESC	embryonic stem cell:	n/a	chr18:43912943-43912952 chr18:43913176-43913186
40	MAX	chr18:43912978-43913739	H1-hESC	embryonic stem cell:	n/a	chr18:43913176-43913186
41	MAX	chr18:43912812-43914433	ECC-1	luminal epithelium:	n/a	chr18:43912943-43912952 chr18:43913176-43913186
42	MAX	chr18:43913351-43913855	SK-N-SH	brain:	n/a	n/a
43	MAX	chr18:43912875-43914133	H1-hESC	embryonic stem cell:	n/a	chr18:43912943-43912952 chr18:43913176-43913186
44	MAX	chr18:43913304-43914088	A549	lung:	n/a	n/a
45	MAX	chr18:43912856-43914148	HCT-116	colon:	n/a	chr18:43912943-43912952 chr18:43913176-43913186
46	MAX	chr18:43912966-43913257	K562	blood:	n/a	chr18:43913176-43913186
47	MAX	chr18:43912826-43914017	ECC-1	luminal epithelium:	n/a	chr18:43912943-43912952 chr18:43913176-43913186
48	MAX	chr18:43912992-43913258	NB4	blood:	n/a	chr18:43913176-43913186
49	MAX	chr18:43912986-43914086	Hela-S3	cervix:	n/a	chr18:43913176-43913186
50	MAX	chr18:43913557-43913581	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:43913147-43913197	K562	blood:	n/a
2	chr18:43913147-43913197	SK-N-MC	brain:	n/a
3	chr18:43913147-43913197	Hepatocyte	liver:	n/a
4	chr18:43913346-43913396	HCM	heart:	n/a
5	chr18:43913147-43913197	HRE	kidney:	n/a
6	chr18:43913147-43913197	K562	blood:	n/a
7	chr18:43913147-43913197	SK-N-MC	brain:	n/a
8	chr18:43913147-43913197	Hepatocyte	liver:	n/a
9	chr18:43913346-43913396	HCM	heart:	n/a
10	chr18:43913147-43913197	HRE	kidney:	n/a
11	chr18:43914047-43914097	CMK	blood:	n/a
12	chr18:43913565-43913615	GM19239	blood:	n/a
13	chr18:43913755-43913805	MCF-7	breast:	n/a
14	chr18:43913565-43913615	MCF10A-Er-Src	breast:	n/a
15	chr18:43913699-43913749	BJ	skin:	n/a
16	chr18:43914047-43914097	AG04449	skin:	fetal
17	chr18:43913649-43913699	NT2-D1	testis:	n/a
18	chr18:43913755-43913805	AG04450	lung:	fetal
19	chr18:43913147-43913197	CMK	blood:	n/a
20	chr18:43913147-43913197	HNPCEpiC	eye:	n/a
21	chr18:43913565-43913615	A549	lung:	n/a
22	chr18:43913565-43913615	Jurkat	blood:	n/a
23	chr18:43913719-43913769	MCF-7	breast:	n/a
24	chr18:43913147-43913197	GM12892	blood:	n/a
25	chr18:43913649-43913699	Hela-S3	cervix:	n/a
26	chr18:43913719-43913769	IMR90	lung:	fetal
27	chr18:43913147-43913197	HCT-116	colon:	n/a
28	chr18:43913147-43913197	NH-A	brain:	n/a
29	chr18:43913699-43913749	AG09319	gingival:	n/a
30	chr18:43913346-43913396	NB4	blood:	n/a
31	chr18:43913346-43913396	BJ	skin:	n/a
32	chr18:43913649-43913699	LNCaP	prostate:	n/a
33	chr18:43914047-43914097	HMEC	breast:	n/a
34	chr18:43913565-43913615	BJ	skin:	n/a
35	chr18:43913699-43913749	HCPEpiC	choroid plexus:	n/a
36	chr18:43913719-43913769	HCF	heart:	n/a
37	chr18:43913147-43913197	HMEC	breast:	n/a
38	chr18:43913565-43913615	HCM	heart:	n/a
39	chr18:43913147-43913197	MCF-7	breast:	n/a
40	chr18:43913719-43913769	H1-hESC	embryonic stem cell:	embryo
41	chr18:43913755-43913805	IMR90	lung:	fetal
42	chr18:43913719-43913769	HAEpiC	amniotic membrane:	n/a
43	chr18:43913565-43913615	AG04449	skin:	fetal
44	chr18:43914047-43914097	HRE	kidney:	n/a
45	chr18:43913346-43913396	LNCaP	prostate:	n/a
46	chr18:43913649-43913699	HPAEpiC	pulmonary alveolar:	n/a
47	chr18:43913346-43913396	HCF	heart:	n/a
48	chr18:43913649-43913699	H1-hESC	embryonic stem cell:	embryo
49	chr18:43914047-43914097	PrEC	prostate:	n/a
50	chr18:43913719-43913769	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:43912035..43913739-chr18:43924023..43926965,2	MCF-7	breast:
2	chr18:43751486..43754394-chr18:43913234..43915228,2	MCF-7	breast:
3	chr18:43908257..43911252-chr18:43912177..43914068,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF165-1	chr18:43913931-43914088	NONHSAT059132

Variant related genes	Relation type
RNF165	TF binding region
RNF165	CpG island
ENSG00000152242	chromatin interactions
ENSG00000141622	chromatin interactions

Extended variants
information (count: 101 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:101 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7232125	chr18:43910908-43910909	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556426624	chr18:43911030-43911031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577821222	chr18:43911113-43911114	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs113276041	chr18:43911115-43911116	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs545319050	chr18:43911178-43911179	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs560417228	chr18:43911190-43911191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs527465135	chr18:43911281-43911282	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs150978403	chr18:43911311-43911312	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs560792154	chr18:43911364-43911365	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs531336839	chr18:43911443-43911444	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs11082521	chr18:43911448-43911449	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs72907334	chr18:43911545-43911546	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs533494161	chr18:43911546-43911547	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs551639323	chr18:43911567-43911568	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs537368810	chr18:43911606-43911607	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs11082522	chr18:43911621-43911622	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs56958501	chr18:43911658-43911659	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs140848784	chr18:43911673-43911674	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs555463199	chr18:43911684-43911685	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs190082314	chr18:43911685-43911686	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs550490423	chr18:43911717-43911718	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs181499756	chr18:43911736-43911737	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs556329535	chr18:43911752-43911753	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs184213075	chr18:43911753-43911754	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs188498831	chr18:43911773-43911774	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs149689818	chr18:43911779-43911780	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs572289002	chr18:43911856-43911857	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs181070792	chr18:43911876-43911877	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs59547583	chr18:43911877-43911878	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs549562192	chr18:43911896-43911897	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs185920901	chr18:43911962-43911963	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs75442330	chr18:43911984-43911985	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566166054	chr18:43912014-43912015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373420536	chr18:43912041-43912042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543503962	chr18:43912108-43912109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564758096	chr18:43912112-43912113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531969127	chr18:43912232-43912233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75188192	chr18:43912233-43912234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140290495	chr18:43912258-43912259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527738086	chr18:43912274-43912275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192438846	chr18:43912286-43912287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567840315	chr18:43912306-43912307	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs145199111	chr18:43912343-43912344	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs375989399	chr18:43912345-43912346	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs137890331	chr18:43912349-43912350	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs182006813	chr18:43912375-43912376	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs539006605	chr18:43912426-43912427	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs533838316	chr18:43912445-43912446	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs572325312	chr18:43912482-43912483	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs536539305	chr18:43912483-43912484	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
low-grade B-cell lymphoma tumor	18367492	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
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	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
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:43906000-43912400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr18:43906000-43912400	Weak transcription	Hela-S3	cervix
3	chr18:43911000-43912600	Enhancers	Liver	Liver
4	chr18:43911200-43911600	Enhancers	HepG2	liver
5	chr18:43911200-43911600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
6	chr18:43911400-43911600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
7	chr18:43911600-43912000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr18:43912200-43912800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr18:43912200-43913200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr18:43912400-43912800	Enhancers	Hela-S3	cervix
11	chr18:43912400-43913000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr18:43912400-43913000	Enhancers	Fetal Brain Male	brain
13	chr18:43912400-43913000	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr18:43912400-43913200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr18:43912400-43913400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr18:43912400-43913400	Enhancers	Right Ventricle	heart
17	chr18:43912600-43912800	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr18:43912600-43912800	Enhancers	Fetal Brain Female	brain
19	chr18:43912600-43912800	Enhancers	Dnd41	blood
20	chr18:43912600-43913000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
21	chr18:43912600-43913200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
22	chr18:43912600-43913200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
23	chr18:43912600-43913200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr18:43912600-43913400	Enhancers	Placenta Amnion	Placenta Amnion
25	chr18:43912600-43913800	Flanking Active TSS	Liver	Liver
26	chr18:43912800-43913000	Enhancers	Brain Anterior Caudate	brain
27	chr18:43912800-43913000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
28	chr18:43912800-43913000	Enhancers	Brain Substantia Nigra	brain
29	chr18:43912800-43913000	Enhancers	Esophagus	oesophagus
30	chr18:43912800-43913000	Flanking Active TSS	Fetal Brain Female	brain
31	chr18:43912800-43913000	Enhancers	Fetal Heart	heart
32	chr18:43912800-43913200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
33	chr18:43912800-43913200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr18:43912800-43913200	Bivalent Enhancer	Fetal Lung	lung
35	chr18:43912800-43913200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr18:43912800-43913200	Bivalent Enhancer	Fetal Muscle Leg	muscle
37	chr18:43912800-43913400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr18:43912800-43913400	Enhancers	Left Ventricle	heart
39	chr18:43912800-43913400	Enhancers	Pancreas	Pancrea
40	chr18:43912800-43913400	Enhancers	Right Atrium	heart
41	chr18:43912800-43913600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr18:43912800-43913600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr18:43912800-43913600	Flanking Active TSS	Hela-S3	cervix
44	chr18:43912800-43913800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
45	chr18:43912800-43913800	Flanking Active TSS	Dnd41	blood
46	chr18:43912800-43915000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
47	chr18:43912800-43915800	Active TSS	Brain Cingulate Gyrus	brain
48	chr18:43913000-43913200	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr18:43913000-43913200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr18:43913000-43913200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell

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