Variant report

Variant	nsv431976
Chromosome Location	chr18:30129553-30194102
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	ARID3A	chr18:30131174-30131190	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:30142422-30142500	HepG2	liver:	n/a	n/a
3	BACH1	chr18:30190420-30190421	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr18:30178218-30178457	GM12878	blood:	n/a	n/a
5	BHLHE40	chr18:30132459-30132771	GM12878	blood:	n/a	n/a
6	CEBPB	chr18:30159138-30159403	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr18:30146615-30146815	A549	lung:	n/a	n/a
8	CEBPB	chr18:30141181-30141299	HepG2	liver:	n/a	chr18:30141235-30141246
9	CEBPB	chr18:30193391-30193636	IMR90	lung:	n/a	chr18:30193474-30193485
10	CEBPB	chr18:30193371-30193687	HepG2	liver:	n/a	chr18:30193474-30193485
11	CEBPB	chr18:30157849-30158073	HepG2	liver:	n/a	chr18:30157971-30157982
12	CEBPB	chr18:30157855-30158133	IMR90	lung:	n/a	chr18:30157971-30157982
13	CEBPB	chr18:30193453-30193677	A549	lung:	n/a	chr18:30193474-30193485
14	CHD2	chr18:30132430-30132793	HepG2	liver:	n/a	n/a
15	CHD2	chr18:30136205-30136420	K562	blood:	n/a	n/a
16	CHD2	chr18:30130908-30131239	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr18:30129211-30129650	H1-hESC	embryonic stem cell:	n/a	chr18:30129418-30129431
18	CTCF	chr18:30156280-30156552	H1-hESC	embryonic stem cell:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
19	CTCF	chr18:30156380-30156530	AG04450	lung:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
20	CTCF	chr18:30132374-30132721	MCF-7	breast:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
21	CTCF	chr18:30130997-30131230	MCF-7	breast:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
22	CTCF	chr18:30156400-30156550	GM12872	blood:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
23	CTCF	chr18:30156420-30156570	GM12864	blood:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
24	CTCF	chr18:30132472-30132732	Hela-S3	cervix:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
25	CTCF	chr18:30131072-30131145	HUVEC	blood vessel:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
26	CTCF	chr18:30132820-30132970	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr18:30132520-30132670	HCT-116	colon:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
28	CTCF	chr18:30132540-30132690	BJ	skin:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
29	CTCF	chr18:30156340-30156490	GM12867	blood:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
30	CTCF	chr18:30132840-30132990	GM12872	blood:	n/a	n/a
31	CTCF	chr18:30132520-30132670	HCPEpiC	choroid plexus:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
32	CTCF	chr18:30156369-30156537	MCF-7	breast:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
33	CTCF	chr18:30132520-30132670	BE2_C	brain:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
34	CTCF	chr18:30132940-30133090	GM12865	blood:	n/a	n/a
35	CTCF	chr18:30130960-30131110	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr18:30156320-30156470	MCF-7	breast:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
37	CTCF	chr18:30132500-30132650	HEK293	kidney:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
38	CTCF	chr18:30131000-30131150	AG04449	skin:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
39	CTCF	chr18:30132449-30132744	Spleen_OC	spleen:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
40	CTCF	chr18:30156389-30156558	GM19240	blood:	n/a	chr18:30156435-30156453 chr18:30156438-30156451 chr18:30156438-30156447
41	CTCF	chr18:30156140-30156410	K562	blood:	n/a	n/a
42	CTCF	chr18:30132460-30132610	GM12801	blood:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
43	CTCF	chr18:30131060-30131210	AoAF	blood vessel:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
44	CTCF	chr18:30132465-30132732	K562	blood:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
45	CTCF	chr18:30131020-30131170	K562	blood:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
46	CTCF	chr18:30132435-30132747	HUVEC	blood vessel:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
47	CTCF	chr18:30131060-30131210	HMF	breast:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
48	CTCF	chr18:30131000-30131150	HPAF	blood vessel:	n/a	chr18:30131109-30131122 chr18:30131110-30131119
49	CTCF	chr18:30132327-30132810	HepG2	liver:	n/a	chr18:30132580-30132596 chr18:30132579-30132597 chr18:30132585-30132594
50	CTCF	chr18:30131040-30131190	AG04450	lung:	n/a	chr18:30131109-30131122 chr18:30131110-30131119

No.	Distal block	Cell Line	Cell type
1	chr18:30155938..30156890-chr18:30249254..30250445,9	MCF-7	breast:
2	chr18:29737793..29738341-chr18:30132122..30132837,2	MCF-7	breast:
3	chr18:30188889..30190990-chr18:30209240..30211617,2	MCF-7	breast:
4	chr18:30156031..30156847-chr18:30254282..30255103,2	MCF-7	breast:
5	chr18:30125345..30127193-chr18:30127513..30129588,2	MCF-7	breast:
6	chr18:30124765..30126879-chr18:30130825..30132479,2	MCF-7	breast:
7	chr18:30156679..30157193-chr18:30249087..30249714,2	MCF-7	breast:
8	chr18:29737713..29738256-chr18:30129386..30129926,2	MCF-7	breast:
9	chr18:30049439..30053878-chr18:30126244..30131084,5	MCF-7	breast:
10	chr18:29737731..29738647-chr18:30131030..30131759,2	MCF-7	breast:
11	chr18:30049677..30051378-chr18:30146420..30148421,2	MCF-7	breast:
12	chr18:30132180..30132981-chr18:30253686..30254646,2	MCF-7	breast:
13	chr18:29913485..29914461-chr18:30129286..30129947,2	MCF-7	breast:
14	chr18:29737720..29738653-chr18:30132086..30132779,5	K562	blood:
15	chr18:29869178..29870066-chr18:30128854..30129812,2	MCF-7	breast:
16	chr18:29851552..29852413-chr18:30132133..30133147,4	MCF-7	breast:
17	chr18:29737738..29738425-chr18:30129431..30129978,2	MCF-7	breast:
18	chr18:29737699..29739046-chr18:30132133..30133008,6	MCF-7	breast:
19	chr18:29869293..29870126-chr18:30132476..30133178,2	MCF-7	breast:
20	chr18:30133804..30136376-chr18:30138480..30140813,2	MCF-7	breast:
21	chr18:30190203..30191854-chr18:30213352..30215090,2	MCF-7	breast:
22	chr18:30133804..30136376-chr18:30138480..30140813,2	MCF-7	breast:
23	chr18:29851628..29852386-chr18:30132192..30133063,2	MCF-7	breast:
24	chr18:29851159..29852631-chr18:30128814..30129900,6	MCF-7	breast:
25	chr18:30155970..30156491-chr18:30499440..30500054,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC012123.1.1-3	chr18:30161491-30161539	ENSG00000263688.1
2	lnc-AC012123.1.1-3	chr18:30162577-30162791	ENSG00000263688.1

Variant related genes	Relation type
ENSG00000263688	TF binding region
ENSG00000141441	chromatin interactions

Extended variants
information (count: 1019 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1019 , 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	rs16963547	chr18:30129553-30129554	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs330988	chr18:30129575-30129576	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs150927777	chr18:30129614-30129615	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557333515	chr18:30129626-30129627	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs554634800	chr18:30129643-30129644	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs9964350	chr18:30129645-30129646	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs540093005	chr18:30129691-30129692	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs79516225	chr18:30129725-30129726	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs74717751	chr18:30129770-30129771	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs556429130	chr18:30129831-30129832	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544037155	chr18:30129897-30129898	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs543285288	chr18:30129971-30129972	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs562223452	chr18:30129989-30129990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs529720163	chr18:30130028-30130029	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10468906	chr18:30130075-30130076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs372182372	chr18:30130127-30130128	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs74861942	chr18:30130160-30130161	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs547301645	chr18:30130162-30130163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs79003532	chr18:30130245-30130246	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs330987	chr18:30130249-30130250	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs376518409	chr18:30130280-30130281	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573811440	chr18:30130281-30130282	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs188468312	chr18:30130357-30130358	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs373345323	chr18:30130358-30130359	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs373837647	chr18:30130368-30130369	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs140671858	chr18:30130394-30130395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs200323551	chr18:30130404-30130405	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs143293167	chr18:30130458-30130459	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs555050245	chr18:30130459-30130460	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs146681589	chr18:30130491-30130492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs540272114	chr18:30130498-30130499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs1613270	chr18:30130500-30130501	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558414360	chr18:30130508-30130509	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576755461	chr18:30130509-30130510	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs376767228	chr18:30130516-30130517	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs140363036	chr18:30130519-30130520	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532245923	chr18:30130561-30130562	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs35790395	chr18:30130577-30130578	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs536053574	chr18:30130578-30130579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs79780030	chr18:30130592-30130593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs76753288	chr18:30130593-30130594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs330986	chr18:30130609-30130610	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560232575	chr18:30130610-30130611	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs527260642	chr18:30130618-30130619	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs145449183	chr18:30130661-30130662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs138150702	chr18:30130710-30130711	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532823142	chr18:30130718-30130719	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551308196	chr18:30130722-30130723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs569307933	chr18:30130747-30130748	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs369998135	chr18:30130784-30130785	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
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
Glioblastoma multiforme	21922591	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
Lung cancer	18438408	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
Hepatocellular carcinoma	16750200	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
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:144 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30122600-30133200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr18:30128000-30130200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr18:30128200-30129800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr18:30128200-30130000	Enhancers	H1 Cell Line	embryonic stem cell
5	chr18:30128400-30129800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr18:30128600-30130000	Enhancers	Fetal Brain Male	brain
7	chr18:30128600-30130200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr18:30128800-30131000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr18:30128800-30133000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr18:30129000-30129800	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr18:30129000-30129800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr18:30129000-30129800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr18:30129000-30131000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr18:30129000-30131200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr18:30129000-30132400	Weak transcription	Stomach Mucosa	stomach
16	chr18:30129000-30133600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr18:30129200-30130200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr18:30129200-30132800	Weak transcription	Fetal Intestine Small	intestine
19	chr18:30129800-30130800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr18:30129800-30130800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr18:30129800-30130800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr18:30129800-30130800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr18:30129800-30130800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr18:30130000-30130400	Weak transcription	Fetal Brain Male	brain
25	chr18:30130000-30131000	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr18:30130200-30130600	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr18:30130200-30130600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr18:30130200-30131600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr18:30130400-30131200	Enhancers	Fetal Brain Male	brain
30	chr18:30130600-30131600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr18:30130600-30131800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr18:30130800-30131200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr18:30130800-30131200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr18:30130800-30131200	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr18:30130800-30131400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr18:30130800-30131800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr18:30130800-30131800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr18:30131000-30131200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr18:30131000-30131200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
40	chr18:30131000-30131400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr18:30131000-30131800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr18:30131000-30131800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr18:30131200-30131400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr18:30131200-30131600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr18:30131200-30132800	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr18:30131200-30136400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr18:30131400-30133000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr18:30131400-30133200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr18:30131600-30131800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr18:30131600-30132000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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