Variant report

Variant	esv2752385
Chromosome Location	chr9:71304465-71332240
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	chr9:71320671-71320784	K562	blood:	n/a	n/a
2	ARID3A	chr9:71319857-71320037	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:71313920-71314482	K562	blood:	n/a	n/a
4	ARID3A	chr9:71317436-71317732	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:71319020-71319266	K562	blood:	n/a	n/a
6	ARID3A	chr9:71321237-71321426	HepG2	liver:	n/a	n/a
7	ATF1	chr9:71314125-71314344	K562	blood:	n/a	n/a
8	ATF2	chr9:71321421-71322309	GM12878	blood:	n/a	n/a
9	ATF2	chr9:71321325-71322566	GM12878	blood:	n/a	n/a
10	BACH1	chr9:71320813-71321013	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr9:71319184-71319411	K562	blood:	n/a	n/a
12	BACH1	chr9:71319599-71320156	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr9:71314082-71314261	K562	blood:	n/a	n/a
14	BACH1	chr9:71317454-71317734	K562	blood:	n/a	n/a
15	BATF	chr9:71321805-71322154	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:71321556-71321816	GM12878	blood:	n/a	chr9:71321721-71321730
17	BCL11A	chr9:71321536-71322089	GM12878	blood:	n/a	chr9:71321721-71321730
18	BCL3	chr9:71319918-71320321	GM12878	blood:	n/a	chr9:71320125-71320138 chr9:71320133-71320146 chr9:71319925-71319938 chr9:71319926-71319939 chr9:71320127-71320140 chr9:71320211-71320224 chr9:71320141-71320154 chr9:71320265-71320278 chr9:71319930-71319939
19	BCL3	chr9:71321460-71322211	GM12878	blood:	n/a	chr9:71321721-71321730
20	BCLAF1	chr9:71321217-71322244	GM12878	blood:	n/a	chr9:71321721-71321730
21	BCLAF1	chr9:71319996-71320510	GM12878	blood:	n/a	chr9:71320125-71320138 chr9:71320133-71320146 chr9:71320127-71320140 chr9:71320211-71320224 chr9:71320141-71320154 chr9:71320461-71320474 chr9:71320265-71320278
22	BCLAF1	chr9:71321438-71322246	GM12878	blood:	n/a	chr9:71321721-71321730
23	BCLAF1	chr9:71319813-71320483	GM12878	blood:	n/a	chr9:71320125-71320138 chr9:71320133-71320146 chr9:71319925-71319938 chr9:71319926-71319939 chr9:71320127-71320140 chr9:71320211-71320224 chr9:71320141-71320154 chr9:71320461-71320474 chr9:71320265-71320278 chr9:71319930-71319939
24	BHLHE40	chr9:71323217-71323744	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:71321464-71322514	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:71319893-71320254	GM12878	blood:	n/a	chr9:71320130-71320146 chr9:71320133-71320149 chr9:71320214-71320230 chr9:71320125-71320141
27	BHLHE40	chr9:71320806-71321476	K562	blood:	n/a	n/a
28	BHLHE40	chr9:71319789-71320453	K562	blood:	n/a	chr9:71320130-71320146 chr9:71320133-71320149 chr9:71320214-71320230 chr9:71320125-71320141
29	BHLHE40	chr9:71319903-71320790	HepG2	liver:	n/a	chr9:71320130-71320146 chr9:71320133-71320149 chr9:71320214-71320230 chr9:71320125-71320141
30	BHLHE40	chr9:71316803-71316805	K562	blood:	n/a	n/a
31	BHLHE40	chr9:71320803-71321003	GM12878	blood:	n/a	n/a
32	BHLHE40	chr9:71312716-71313047	K562	blood:	n/a	n/a
33	BHLHE40	chr9:71314074-71314371	K562	blood:	n/a	n/a
34	BHLHE40	chr9:71317542-71317628	K562	blood:	n/a	n/a
35	CBX3	chr9:71319837-71320191	K562	blood:	n/a	n/a
36	CCNT2	chr9:71319615-71321391	K562	blood:	n/a	chr9:71319903-71319912 chr9:71320696-71320705 chr9:71321382-71321391
37	CEBPB	chr9:71320542-71320863	MCF-7	breast:	n/a	n/a
38	CEBPB	chr9:71319650-71319670	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr9:71320535-71320759	K562	blood:	n/a	n/a
40	CEBPB	chr9:71321296-71322449	GM12878	blood:	n/a	n/a
41	CEBPB	chr9:71320451-71320843	K562	blood:	n/a	n/a
42	CEBPB	chr9:71320551-71320727	HepG2	liver:	n/a	n/a
43	CEBPB	chr9:71312925-71313204	K562	blood:	n/a	n/a
44	CEBPB	chr9:71320492-71320791	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr9:71319953-71320174	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr9:71320457-71320811	HepG2	liver:	n/a	n/a
47	CEBPB	chr9:71319855-71320846	HepG2	liver:	n/a	n/a
48	CEBPB	chr9:71304689-71304980	HepG2	liver:	n/a	chr9:71304821-71304832 chr9:71304821-71304834 chr9:71304823-71304834
49	CEBPB	chr9:71304699-71304965	IMR90	lung:	n/a	chr9:71304821-71304832 chr9:71304821-71304834 chr9:71304823-71304834
50	CEBPB	chr9:71319901-71320191	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71316119-71316169	AG04450	lung:	fetal
2	chr9:71316119-71316169	AG04450	lung:	fetal
3	chr9:71320601-71320651	K562	blood:	n/a
4	chr9:71320671-71320721	PFSK-1	brain:	n/a
5	chr9:71319485-71319535	AG04450	lung:	fetal
6	chr9:71319771-71319821	GM12891	blood:	n/a
7	chr9:71319485-71319535	HUVEC	blood vessel:	n/a
8	chr9:71320693-71320743	HepG2	liver:	n/a
9	chr9:71319771-71319821	IMR90	lung:	fetal
10	chr9:71320601-71320651	HMEC	breast:	n/a
11	chr9:71319485-71319535	U87	brain:	n/a
12	chr9:71320601-71320651	MCF10A-Er-Src	breast:	n/a
13	chr9:71319485-71319535	BE2_C	brain:	n/a
14	chr9:71316119-71316169	BJ	skin:	n/a
15	chr9:71319485-71319535	GM12878	blood:	n/a
16	chr9:71320601-71320651	NHDF-neo	bronchial:	n/a
17	chr9:71319356-71319406	SKMC	muscle:	n/a
18	chr9:71316119-71316169	T-47D	breast:	n/a
19	chr9:71319485-71319535	BJ	skin:	n/a
20	chr9:71319485-71319535	K562	blood:	n/a
21	chr9:71319771-71319821	H1-hESC	embryonic stem cell:	embryo
22	chr9:71320671-71320721	BE2_C	brain:	n/a
23	chr9:71319771-71319821	SKMC	muscle:	n/a
24	chr9:71320601-71320651	AG09309	skin:	n/a
25	chr9:71319771-71319821	PrEC	prostate:	n/a
26	chr9:71320601-71320651	HRPEpiC	eye:	n/a
27	chr9:71316119-71316169	GM12891	blood:	n/a
28	chr9:71320693-71320743	AG09319	gingival:	n/a
29	chr9:71319485-71319535	HEK293	kidney:	embryo
30	chr9:71316119-71316169	NH-A	brain:	n/a
31	chr9:71320693-71320743	HIPEpiC	eye:	n/a
32	chr9:71319771-71319821	CMK	blood:	n/a
33	chr9:71320693-71320743	MCF-7	breast:	n/a
34	chr9:71320601-71320651	ovcar-3	ovarian:	n/a
35	chr9:71320601-71320651	GM19239	blood:	n/a
36	chr9:71320693-71320743	HL-60	blood:	n/a
37	chr9:71320671-71320721	AG04449	skin:	fetal
38	chr9:71319485-71319535	SKMC	muscle:	n/a
39	chr9:71319485-71319535	ovcar-3	ovarian:	n/a
40	chr9:71319485-71319535	HAEpiC	amniotic membrane:	n/a
41	chr9:71320693-71320743	PFSK-1	brain:	n/a
42	chr9:71320601-71320651	HCT-116	colon:	n/a
43	chr9:71319771-71319821	Caco-2	colon:	n/a
44	chr9:71319485-71319535	HCM	heart:	n/a
45	chr9:71319485-71319535	T-47D	breast:	n/a
46	chr9:71320693-71320743	IMR90	lung:	fetal
47	chr9:71319771-71319821	BJ	skin:	n/a
48	chr9:71319356-71319406	HCPEpiC	choroid plexus:	n/a
49	chr9:71319356-71319406	H1-hESC	embryonic stem cell:	embryo
50	chr9:71320671-71320721	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:71318773..71321660-chr9:71357020..71360216,3	K562	blood:
2	chr9:71319095..71321406-chr9:71328532..71331423,2	K562	blood:
3	chr9:71320129..71321713-chr9:71324484..71326376,3	K562	blood:
4	chr9:71314661..71316622-chr9:71318012..71320131,2	MCF-7	breast:
5	chr9:71317900..71319915-chr9:71391633..71393560,2	K562	blood:
6	chr9:71317469..71321528-chr9:71322199..71324795,3	MCF-7	breast:
7	chr9:71314661..71316622-chr9:71318012..71320131,2	MCF-7	breast:
8	chr9:71318947..71321633-chr9:71353997..71355633,2	MCF-7	breast:
9	chr9:71208704..71211191-chr9:71318423..71320358,2	MCF-7	breast:
10	chr9:71329696..71331473-chr9:71338572..71340155,2	K562	blood:
11	chr9:71199401..71199961-chr9:71318970..71319652,2	MCF-7	breast:
12	chr9:71314200..71316006-chr9:71392467..71395218,2	K562	blood:
13	chr9:71199033..71199728-chr9:71318176..71318881,4	MCF-7	breast:
14	chr9:71307012..71309934-chr9:71319801..71321541,3	MCF-7	breast:
15	chr9:71324675..71326449-chr9:71333129..71335717,2	K562	blood:
16	chr9:71312864..71316000-chr9:71317726..71321566,4	MCF-7	breast:
17	chr9:71317604..71326808-chr9:71328532..71337502,16	K562	blood:
18	chr9:71319577..71321555-chr9:71393458..71395334,2	MCF-7	breast:
19	chr9:71318506..71320929-chr9:71321155..71324459,4	K562	blood:
20	chr9:71320513..71323388-chr9:71323733..71326341,2	MCF-7	breast:
21	chr9:71316561..71319400-chr9:71390897..71393133,2	K562	blood:
22	chr9:71310655..71314334-chr9:71315836..71317946,3	K562	blood:
23	chr9:71318556..71321196-chr9:71331205..71333061,2	MCF-7	breast:
24	chr9:71329093..71331549-chr9:71334294..71336227,2	K562	blood:
25	chr9:71313421..71317704-chr9:71318350..71323636,8	K562	blood:
26	chr9:71316265..71319270-chr9:71393472..71396544,3	MCF-7	breast:
27	chr9:71310655..71314334-chr9:71315836..71317946,3	K562	blood:
28	chr9:71304980..71307129-chr9:71354000..71355533,2	MCF-7	breast:
29	chr9:71319203..71320145-chr9:71614622..71615180,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM122A-1	chr9:71320902-71321138	NONHSAT131754
2	lnc-FAM122A-1	chr9:71322519-71323057	NONHSAT131754
3	lnc-FAM122A-1	chr9:71320901-71321138	NONHSAT131753

Variant related genes	Relation type
PIP5K1B	TF binding region
PIP5K1B	CpG island
ENSG00000107242	chromatin interactions
ENSG00000187866	chromatin interactions

Extended variants
information (count: 920 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:920 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11143413	chr9:71304465-71304466	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11143414	chr9:71304548-71304549	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs537976369	chr9:71304585-71304586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184208911	chr9:71304619-71304620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140860005	chr9:71304631-71304632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11143415	chr9:71304649-71304650	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs553795795	chr9:71304675-71304676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373172278	chr9:71304684-71304685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs59193953	chr9:71304706-71304707	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs542416203	chr9:71304769-71304770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190004054	chr9:71304777-71304778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs11143417	chr9:71304812-71304813	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs180836403	chr9:71304821-71304822	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs562880555	chr9:71304851-71304852	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs564469401	chr9:71304902-71304903	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs186185110	chr9:71304917-71304918	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs533273834	chr9:71304950-71304951	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs574217778	chr9:71304986-71304987	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs12338099	chr9:71305001-71305002	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs191907667	chr9:71305004-71305005	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs549586638	chr9:71305050-71305051	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs567904266	chr9:71305072-71305073	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs559533615	chr9:71305077-71305078	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs537916708	chr9:71305140-71305141	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560213341	chr9:71305187-71305188	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs556018990	chr9:71305219-71305220	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs11999940	chr9:71305241-71305242	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs182442823	chr9:71305245-71305246	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs538278008	chr9:71305246-71305247	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs553985797	chr9:71305247-71305248	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200342074	chr9:71305271-71305272	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs549152649	chr9:71305272-71305273	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185763636	chr9:71305273-71305274	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554341484	chr9:71305276-71305277	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs574949920	chr9:71305277-71305278	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs575862007	chr9:71305312-71305313	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs372495323	chr9:71305319-71305320	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs544679081	chr9:71305365-71305366	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562859233	chr9:71305374-71305375	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs533333753	chr9:71305379-71305380	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs543568222	chr9:71305393-71305394	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs560510025	chr9:71305395-71305396	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs77296351	chr9:71305398-71305399	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190520126	chr9:71305410-71305411	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs150140667	chr9:71305450-71305451	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs531956696	chr9:71305460-71305461	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs138872252	chr9:71305473-71305474	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182401647	chr9:71305485-71305486	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141321935	chr9:71305531-71305532	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs73646757	chr9:71305533-71305534	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Bipolar disorder	19214233	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:763 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71303200-71308400	Enhancers	Fetal Heart	heart
2	chr9:71303400-71306800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:71303800-71306600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr9:71304000-71305200	Enhancers	Fetal Intestine Small	intestine
5	chr9:71304000-71305400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr9:71304000-71305400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr9:71304200-71304800	Weak transcription	Left Ventricle	heart
8	chr9:71304400-71304800	Weak transcription	Stomach Mucosa	stomach
9	chr9:71304600-71305000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr9:71304600-71305800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr9:71304800-71305200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr9:71304800-71305200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr9:71304800-71305200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr9:71304800-71305200	Enhancers	HepG2	liver
15	chr9:71304800-71305400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr9:71304800-71305400	Enhancers	Colon Smooth Muscle	Colon
17	chr9:71304800-71305400	Enhancers	Fetal Intestine Large	intestine
18	chr9:71304800-71305400	Enhancers	Left Ventricle	heart
19	chr9:71304800-71305400	Enhancers	Stomach Mucosa	stomach
20	chr9:71304800-71305600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:71304800-71305800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr9:71305000-71305200	Bivalent Enhancer	Esophagus	oesophagus
23	chr9:71305000-71305400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr9:71305200-71305600	Weak transcription	Fetal Intestine Small	intestine
25	chr9:71305400-71308200	Weak transcription	Stomach Mucosa	stomach
26	chr9:71305400-71319400	Weak transcription	Left Ventricle	heart
27	chr9:71305600-71305800	Enhancers	Fetal Intestine Small	intestine
28	chr9:71305800-71318600	Weak transcription	Fetal Intestine Small	intestine
29	chr9:71306200-71306600	Enhancers	Aorta	Aorta
30	chr9:71308000-71308600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr9:71308200-71308800	Enhancers	Stomach Mucosa	stomach
32	chr9:71308400-71311800	Weak transcription	Fetal Heart	heart
33	chr9:71311800-71312200	Enhancers	Fetal Heart	heart
34	chr9:71312200-71312600	Flanking Active TSS	Fetal Heart	heart
35	chr9:71312600-71313600	Enhancers	K562	blood
36	chr9:71312600-71313800	Enhancers	Fetal Heart	heart
37	chr9:71312800-71313000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr9:71312800-71313400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr9:71312800-71313400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr9:71313000-71313200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr9:71313000-71314600	Enhancers	Primary hematopoietic stem cells	blood
42	chr9:71313200-71314000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr9:71313200-71314400	Enhancers	Primary B cells from peripheral blood	blood
44	chr9:71313200-71318600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr9:71313400-71314400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr9:71313600-71313800	Flanking Active TSS	K562	blood
47	chr9:71313600-71314200	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr9:71313800-71314400	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr9:71313800-71314600	Enhancers	K562	blood
50	chr9:71313800-71315600	Weak transcription	Fetal Heart	heart

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