Variant report

Variant	nsv560395
Chromosome Location	chr12:119532430-119558565
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	chr12:119553096-119553503	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr12:119553134-119553434	GM12878	blood:	n/a	n/a
3	CEBPB	chr12:119540060-119540530	MCF-7	breast:	n/a	n/a
4	CTCF	chr12:119552780-119552930	HUVEC	blood vessel:	n/a	n/a
5	CTCF	chr12:119553152-119553412	Pancreas_OC	pancreas:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
6	CTCF	chr12:119553180-119553330	HepG2	liver:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
7	CTCF	chr12:119553220-119553370	Caco-2	colon:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
8	CTCF	chr12:119552961-119553007	Gliobla	brain:	n/a	n/a
9	CTCF	chr12:119553172-119553421	Fibrobl	skin:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
10	CTCF	chr12:119553220-119553370	HCT-116	colon:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
11	CTCF	chr12:119553220-119553370	HepG2	liver:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
12	CTCF	chr12:119553160-119553310	HRE	kidney:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
13	CTCF	chr12:119553188-119553414	GM12892	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
14	CTCF	chr12:119553142-119553416	A549	lung:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
15	CTCF	chr12:119552840-119552990	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr12:119552920-119553070	K562	blood:	n/a	n/a
17	CTCF	chr12:119553200-119553350	GM12864	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
18	CTCF	chr12:119553220-119553370	RPTEC	kidney:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
19	CTCF	chr12:119552951-119553050	GM19238	blood:	n/a	n/a
20	CTCF	chr12:119553141-119553410	LNCaP	prostate:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
21	CTCF	chr12:119553200-119553350	HMEC	breast:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
22	CTCF	chr12:119553220-119553370	GM12865	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
23	CTCF	chr12:119553220-119553370	HRE	kidney:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
24	CTCF	chr12:119553260-119553410	HFF-Myc	foreskin:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
25	CTCF	chr12:119553143-119553406	LNCaP	prostate:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
26	CTCF	chr12:119552981-119553493	IMR90	lung:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
27	CTCF	chr12:119553200-119553350	HCFaa	heart:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
28	CTCF	chr12:119553220-119553370	GM06990	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
29	CTCF	chr12:119553220-119553370	GM12869	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
30	CTCF	chr12:119552840-119552990	GM12873	blood:	n/a	n/a
31	CTCF	chr12:119552907-119553679	A549	lung:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
32	CTCF	chr12:119553240-119553390	HMF	breast:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
33	CTCF	chr12:119553177-119553611	HCT-116	colon:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
34	CTCF	chr12:119553192-119553428	GM19240	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
35	CTCF	chr12:119553092-119553513	K562	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
36	CTCF	chr12:119553200-119553350	HBMEC	blood vessel:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
37	CTCF	chr12:119553220-119553370	GM12872	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
38	CTCF	chr12:119553201-119553405	MCF-7	breast:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
39	CTCF	chr12:119553131-119553437	SK-N-SH_RA	brain:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
40	CTCF	chr12:119552944-119553033	GM12891	blood:	n/a	n/a
41	CTCF	chr12:119553135-119553418	Lung_OC	lung:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
42	CTCF	chr12:119553039-119553646	SK-N-SH	brain:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
43	CTCF	chr12:119553140-119553290	HCM	heart:	n/a	n/a
44	CTCF	chr12:119553177-119553402	GM19239	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
45	CTCF	chr12:119553093-119553419	K562	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
46	CTCF	chr12:119553220-119553370	GM12878	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
47	CTCF	chr12:119553220-119553370	HEEpiC	esophagus:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
48	CTCF	chr12:119553219-119553382	MCF-7	breast:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
49	CTCF	chr12:119553149-119553420	GM13977	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303
50	CTCF	chr12:119553189-119553422	GM19238	blood:	n/a	chr12:119553280-119553298 chr12:119553283-119553296 chr12:119553282-119553303

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:119534133-119534183	NHDF-neo	bronchial:	n/a
2	chr12:119534133-119534183	HUVEC	blood vessel:	n/a
3	chr12:119534133-119534183	NHDF-neo	bronchial:	n/a
4	chr12:119534133-119534183	HUVEC	blood vessel:	n/a
5	chr12:119534133-119534183	HCM	heart:	n/a
6	chr12:119534133-119534183	RPTEC	kidney:	n/a
7	chr12:119534133-119534183	MCF-7	breast:	n/a
8	chr12:119534133-119534183	HRE	kidney:	n/a
9	chr12:119534133-119534183	HCT-116	colon:	n/a
10	chr12:119534133-119534183	AG09309	skin:	n/a
11	chr12:119557318-119557368	GM12892	blood:	n/a
12	chr12:119557318-119557368	NHBE	bronchial:	n/a
13	chr12:119534133-119534183	BJ	skin:	n/a
14	chr12:119534133-119534183	HL-60	blood:	n/a
15	chr12:119534133-119534183	PrEC	prostate:	n/a
16	chr12:119557318-119557368	NH-A	brain:	n/a
17	chr12:119557318-119557368	ovcar-3	ovarian:	n/a
18	chr12:119534133-119534183	AoSMC	blood vessel:	n/a
19	chr12:119557318-119557368	ProgFib	skin:	n/a
20	chr12:119557318-119557368	HRCEpiC	kidney:	n/a
21	chr12:119534133-119534183	HCPEpiC	choroid plexus:	n/a
22	chr12:119557318-119557368	Hela-S3	cervix:	n/a
23	chr12:119557318-119557368	NB4	blood:	n/a
24	chr12:119534133-119534183	AG09319	gingival:	n/a
25	chr12:119557318-119557368	HCPEpiC	choroid plexus:	n/a
26	chr12:119534133-119534183	SAEC	small airway:	n/a
27	chr12:119534133-119534183	MCF10A-Er-Src	breast:	n/a
28	chr12:119557318-119557368	HCF	heart:	n/a
29	chr12:119557318-119557368	MCF10A-Er-Src	breast:	n/a
30	chr12:119557318-119557368	AG09309	skin:	n/a
31	chr12:119534133-119534183	AG10803	skin:	n/a
32	chr12:119557318-119557368	AG04450	lung:	fetal
33	chr12:119557318-119557368	IMR90	lung:	fetal
34	chr12:119557318-119557368	HEEpiC	esophagus:	n/a
35	chr12:119534133-119534183	U87	brain:	n/a
36	chr12:119557318-119557368	HAEpiC	amniotic membrane:	n/a
37	chr12:119557318-119557368	HL-60	blood:	n/a
38	chr12:119557318-119557368	AoSMC	blood vessel:	n/a
39	chr12:119557318-119557368	GM12891	blood:	n/a
40	chr12:119534133-119534183	H1-hESC	embryonic stem cell:	embryo
41	chr12:119534133-119534183	T-47D	breast:	n/a
42	chr12:119534133-119534183	GM06990	blood:	n/a
43	chr12:119534133-119534183	HEK293	kidney:	embryo
44	chr12:119557318-119557368	PANC-1	pancreas:	n/a
45	chr12:119534133-119534183	LNCaP	prostate:	n/a
46	chr12:119557318-119557368	GM06990	blood:	n/a
47	chr12:119557318-119557368	ECC-1	luminal epithelium:	n/a
48	chr12:119557318-119557368	Hepatocyte	liver:	n/a
49	chr12:119557318-119557368	HepG2	liver:	n/a
50	chr12:119557318-119557368	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:119519961..119522229-chr12:119531990..119534794,2	MCF-7	breast:
2	chr12:119540016..119541812-chr12:119547746..119549994,2	K562	blood:
3	chr12:119540016..119541812-chr12:119547746..119549994,2	K562	blood:
4	chr12:119556238..119556739-chr12:119608863..119609678,2	MCF-7	breast:
5	chr12:119552783..119553783-chr12:119712402..119713111,2	MCF-7	breast:
6	chr12:119552810..119553329-chr12:119850727..119851485,3	K562	blood:
7	chr12:119457435..119458229-chr12:119552906..119553464,2	MCF-7	breast:
8	chr12:119552855..119553752-chr12:119850687..119851631,3	MCF-7	breast:
9	chr12:119553688..119557524-chr12:119615179..119619342,9	MCF-7	breast:
10	chr12:119552092..119553800-chr12:119555501..119557752,2	K562	blood:
11	chr12:119552092..119553800-chr12:119555501..119557752,2	K562	blood:
12	chr12:119551723..119553234-chr12:119616700..119619134,2	MCF-7	breast:
13	chr12:119556184..119556805-chr12:119608863..119609678,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CIT-6	chr12:119554692-119554766	ENSG00000257095.1
2	lnc-CIT-10	chr12:119551800-119552682	l_740_chr12:119551799-119562709_brain

Variant related genes	Relation type
SRRM4	TF binding region
ENSG00000257095	TF binding region
SRRM4	CpG island
ENSG00000257095	CpG island
ENSG00000152137	chromatin interactions

Extended variants
information (count: 1118 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1118 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7314453	chr12:119532430-119532431	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576212007	chr12:119532443-119532444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114824627	chr12:119532449-119532450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537749923	chr12:119532451-119532452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150180767	chr12:119532476-119532477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191845370	chr12:119532506-119532507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547161079	chr12:119532540-119532541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77531719	chr12:119532558-119532559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs61938015	chr12:119532560-119532561	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs549348427	chr12:119532564-119532565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561810730	chr12:119532575-119532576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76064038	chr12:119532590-119532591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7295638	chr12:119532609-119532610	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs183917676	chr12:119532616-119532617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571779089	chr12:119532647-119532648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7314733	chr12:119532666-119532667	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs138727198	chr12:119532667-119532668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535849186	chr12:119532678-119532679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555713335	chr12:119532688-119532689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7294852	chr12:119532719-119532720	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs545001454	chr12:119532745-119532746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186750219	chr12:119532875-119532876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554166221	chr12:119532918-119532919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373247440	chr12:119532922-119532923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74465603	chr12:119532935-119532936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530677027	chr12:119532949-119532950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541186256	chr12:119532957-119532958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200666000	chr12:119532962-119532963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7295253	chr12:119532963-119532964	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs543057805	chr12:119532969-119532970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34846140	chr12:119532975-119532976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562775830	chr12:119533033-119533034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201367789	chr12:119533050-119533051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531712623	chr12:119533065-119533066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551836505	chr12:119533112-119533113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148900606	chr12:119533118-119533119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7295542	chr12:119533137-119533138	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs547539356	chr12:119533147-119533148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78864417	chr12:119533152-119533153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191168692	chr12:119533163-119533164	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147022793	chr12:119533208-119533209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35446494	chr12:119533218-119533219	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs11610201	chr12:119533220-119533221	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs558585379	chr12:119533243-119533244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572257299	chr12:119533268-119533269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73213703	chr12:119533352-119533353	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs11064660	chr12:119533380-119533381	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs574667103	chr12:119533404-119533405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551502892	chr12:119533423-119533424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543169635	chr12:119533467-119533468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119521000-119535600	Weak transcription	Fetal Brain Female	brain
2	chr12:119521200-119537400	Weak transcription	Brain Germinal Matrix	brain
3	chr12:119528600-119534400	Weak transcription	Right Atrium	heart
4	chr12:119528800-119534200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:119528800-119534200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr12:119529200-119534400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:119529600-119534400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr12:119531400-119533400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr12:119531400-119535800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr12:119531600-119533600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:119531800-119533000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr12:119532000-119532600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr12:119532000-119532600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:119532600-119534200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr12:119532600-119534400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:119532800-119533000	Enhancers	Fetal Brain Male	brain
17	chr12:119533000-119534200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr12:119533000-119534400	Weak transcription	Fetal Brain Male	brain
19	chr12:119533400-119534000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr12:119533600-119534000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:119534000-119534600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr12:119534000-119535200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:119534200-119535000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr12:119534200-119535200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:119534200-119535200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr12:119534200-119535400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr12:119534200-119535400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr12:119534200-119535400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr12:119534400-119534600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr12:119534400-119534600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr12:119534400-119534600	ZNF genes & repeats	Right Atrium	heart
32	chr12:119534400-119534800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr12:119534400-119535000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr12:119534400-119535200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr12:119534400-119535200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr12:119534400-119535200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr12:119534400-119535200	Enhancers	Fetal Brain Male	brain
38	chr12:119534600-119535000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr12:119534800-119535200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
40	chr12:119535200-119568800	Weak transcription	Fetal Brain Male	brain
41	chr12:119535400-119539000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr12:119535600-119536000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
43	chr12:119535600-119538000	Strong transcription	Fetal Brain Female	brain
44	chr12:119537400-119537800	ZNF genes & repeats	Brain Germinal Matrix	brain
45	chr12:119537800-119540000	Weak transcription	Brain Germinal Matrix	brain
46	chr12:119538000-119544600	Weak transcription	Fetal Brain Female	brain
47	chr12:119538400-119539200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr12:119539000-119539400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr12:119540000-119541400	Strong transcription	Brain Germinal Matrix	brain
50	chr12:119541400-119555800	Weak transcription	Brain Germinal Matrix	brain

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