Variant report

Variant	nsv1040628
Chromosome Location	chr12:40180398-40244001
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:459)
CpG islands
(count:62)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:40200982-40201260	K562	blood:	n/a	n/a
2	ARID3A	chr12:40225740-40226084	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:40225811-40226081	K562	blood:	n/a	n/a
4	ARID3A	chr12:40199534-40199560	K562	blood:	n/a	n/a
5	ATF1	chr12:40233006-40233117	K562	blood:	n/a	n/a
6	ATF2	chr12:40229614-40229974	GM12878	blood:	n/a	n/a
7	BATF	chr12:40229525-40229935	GM12878	blood:	n/a	n/a
8	BATF	chr12:40229548-40229926	GM12878	blood:	n/a	n/a
9	BCL11A	chr12:40229655-40229889	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:40229588-40229877	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:40200931-40201073	K562	blood:	n/a	n/a
12	BHLHE40	chr12:40214181-40214238	K562	blood:	n/a	n/a
13	CEBPB	chr12:40218791-40218939	A549	lung:	n/a	chr12:40218888-40218899
14	CEBPB	chr12:40208473-40208792	A549	lung:	n/a	chr12:40208649-40208660
15	CEBPB	chr12:40207664-40207868	A549	lung:	n/a	chr12:40207818-40207829 chr12:40207818-40207829
16	CEBPB	chr12:40207633-40207951	Hela-S3	cervix:	n/a	chr12:40207818-40207829 chr12:40207818-40207829
17	CEBPB	chr12:40200853-40201073	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr12:40218668-40219008	HepG2	liver:	n/a	chr12:40218888-40218899
19	CEBPB	chr12:40181737-40182470	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:40208483-40208752	Hela-S3	cervix:	n/a	chr12:40208649-40208660
21	CEBPB	chr12:40208471-40208796	IMR90	lung:	n/a	chr12:40208649-40208660
22	CEBPB	chr12:40208494-40208781	K562	blood:	n/a	chr12:40208649-40208660
23	CEBPB	chr12:40218325-40219007	Hela-S3	cervix:	n/a	chr12:40218888-40218899
24	CEBPB	chr12:40208432-40208804	HepG2	liver:	n/a	chr12:40208649-40208660
25	CEBPB	chr12:40218675-40219002	IMR90	lung:	n/a	chr12:40218888-40218899
26	CHD2	chr12:40229371-40229882	GM12878	blood:	n/a	n/a
27	CTCF	chr12:40200900-40201050	HMEC	breast:	n/a	n/a
28	CTCF	chr12:40200940-40201090	HMEC	breast:	n/a	n/a
29	CTCF	chr12:40218508-40218621	GM10266	blood:	n/a	n/a
30	CTCF	chr12:40200960-40201110	HPF	lung:	n/a	n/a
31	CTCF	chr12:40200957-40201091	ProgFib	skin:	n/a	n/a
32	CTCF	chr12:40201000-40201150	Caco-2	colon:	n/a	n/a
33	CTCF	chr12:40200960-40201110	NB4	blood:	n/a	n/a
34	CTCF	chr12:40200960-40201110	GM12870	blood:	n/a	n/a
35	CTCF	chr12:40224720-40224870	A549	lung:	n/a	n/a
36	CTCF	chr12:40197118-40197140	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr12:40200800-40200950	GM12864	blood:	n/a	n/a
38	CTCF	chr12:40200960-40201110	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr12:40218460-40218610	Caco-2	colon:	n/a	n/a
40	CTCF	chr12:40218517-40218614	LNCaP	prostate:	n/a	n/a
41	CTCF	chr12:40200900-40201050	GM12865	blood:	n/a	n/a
42	CTCF	chr12:40200940-40201090	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr12:40197033-40197256	LNCaP	prostate:	n/a	n/a
44	CTCF	chr12:40200817-40201224	SK-N-SH	brain:	n/a	n/a
45	CTCF	chr12:40200956-40201095	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr12:40189367-40189550	LNCaP	prostate:	n/a	n/a
47	CTCF	chr12:40200936-40201153	HepG2	liver:	n/a	n/a
48	CTCF	chr12:40200900-40201050	HVMF	connective:	n/a	n/a
49	CTCF	chr12:40218489-40218616	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr12:40200903-40201154	MCF-7	breast:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40197081-40197131	AG09309	skin:	n/a
2	chr12:40197081-40197131	AG09309	skin:	n/a
3	chr12:40197081-40197131	MCF10A-Er-Src	breast:	n/a
4	chr12:40197081-40197131	HEEpiC	esophagus:	n/a
5	chr12:40197081-40197131	SK-N-SH	brain:	n/a
6	chr12:40197081-40197131	CMK	blood:	n/a
7	chr12:40197081-40197131	LNCaP	prostate:	n/a
8	chr12:40197081-40197131	K562	blood:	n/a
9	chr12:40197081-40197131	Caco-2	colon:	n/a
10	chr12:40197081-40197131	HMEC	breast:	n/a
11	chr12:40197081-40197131	NB4	blood:	n/a
12	chr12:40197081-40197131	NT2-D1	testis:	n/a
13	chr12:40197081-40197131	IMR90	lung:	fetal
14	chr12:40197081-40197131	SKMC	muscle:	n/a
15	chr12:40197081-40197131	HRPEpiC	eye:	n/a
16	chr12:40197081-40197131	U87	brain:	n/a
17	chr12:40197081-40197131	HNPCEpiC	eye:	n/a
18	chr12:40197081-40197131	HepG2	liver:	n/a
19	chr12:40197081-40197131	PrEC	prostate:	n/a
20	chr12:40197081-40197131	PFSK-1	brain:	n/a
21	chr12:40197081-40197131	HRE	kidney:	n/a
22	chr12:40197081-40197131	NHDF-neo	bronchial:	n/a
23	chr12:40197081-40197131	BE2_C	brain:	n/a
24	chr12:40197081-40197131	AG09319	gingival:	n/a
25	chr12:40197081-40197131	HPAEpiC	pulmonary alveolar:	n/a
26	chr12:40197081-40197131	H1-hESC	embryonic stem cell:	embryo
27	chr12:40197081-40197131	GM12891	blood:	n/a
28	chr12:40197081-40197131	NHBE	bronchial:	n/a
29	chr12:40197081-40197131	Hepatocyte	liver:	n/a
30	chr12:40197081-40197131	GM12892	blood:	n/a
31	chr12:40197081-40197131	GM19239	blood:	n/a
32	chr12:40197081-40197131	NH-A	brain:	n/a
33	chr12:40197081-40197131	A549	lung:	n/a
34	chr12:40197081-40197131	HCPEpiC	choroid plexus:	n/a
35	chr12:40197081-40197131	SK-N-MC	brain:	n/a
36	chr12:40197081-40197131	Jurkat	blood:	n/a
37	chr12:40197081-40197131	HEK293	kidney:	embryo
38	chr12:40197081-40197131	HCM	heart:	n/a
39	chr12:40197081-40197131	SAEC	small airway:	n/a
40	chr12:40197081-40197131	T-47D	breast:	n/a
41	chr12:40197081-40197131	GM12878	blood:	n/a
42	chr12:40197081-40197131	SK-N-SH_RA	brain:	n/a
43	chr12:40197081-40197131	HIPEpiC	eye:	n/a
44	chr12:40197081-40197131	HUVEC	blood vessel:	n/a
45	chr12:40197081-40197131	HRCEpiC	kidney:	n/a
46	chr12:40197081-40197131	AG10803	skin:	n/a
47	chr12:40197081-40197131	PANC-1	pancreas:	n/a
48	chr12:40197081-40197131	GM06990	blood:	n/a
49	chr12:40197081-40197131	AG04450	lung:	fetal
50	chr12:40197081-40197131	HCT-116	colon:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:40199999..40202917-chr12:40210641..40213494,2	K562	blood:
2	chr12:40233400..40236371-chr12:40236570..40239035,2	MCF-7	breast:
3	chr12:40210443..40213625-chr12:40221266..40224503,3	K562	blood:
4	chr12:40233400..40236371-chr12:40236570..40239035,2	MCF-7	breast:
5	chr12:40239652..40241691-chr12:40246024..40247653,2	K562	blood:
6	chr12:40205089..40207164-chr12:40209269..40211220,2	K562	blood:
7	chr12:40218165..40218758-chr12:40352165..40352674,2	MCF-7	breast:
8	chr12:40210443..40213625-chr12:40221266..40224503,3	K562	blood:
9	chr12:40223815..40226174-chr12:40498333..40500585,2	MCF-7	breast:
10	chr12:40195514..40197262-chr12:40498609..40500773,2	MCF-7	breast:
11	chr12:40224533..40225359-chr12:40351916..40352430,2	MCF-7	breast:
12	chr12:40154023..40155558-chr12:40243257..40245766,2	MCF-7	breast:
13	chr12:40154707..40156485-chr12:40189200..40190990,2	MCF-7	breast:
14	chr12:40199999..40202917-chr12:40210641..40213494,3	K562	blood:
15	chr12:40155001..40155717-chr12:40243633..40244224,2	MCF-7	breast:
16	chr12:40205089..40207164-chr12:40209269..40211220,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000223082	TF binding region
ENSG00000199571	TF binding region
SLC2A13	TF binding region
ENSG00000223082	CpG island
ENSG00000199571	CpG island
SLC2A13	CpG island
ENSG00000223082	chromatin interactions
ENSG00000151229	chromatin interactions

Extended variants
information (count: 2089 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2089 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6581336	chr12:40180398-40180399	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7135047	chr12:40180409-40180410	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs141992233	chr12:40180425-40180426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559654475	chr12:40180448-40180449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111778214	chr12:40180489-40180490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75008895	chr12:40180612-40180613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146302273	chr12:40180647-40180648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs74820408	chr12:40180662-40180663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549017669	chr12:40180673-40180674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6581337	chr12:40180700-40180701	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs370563882	chr12:40180759-40180760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201169429	chr12:40180790-40180791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75531800	chr12:40180798-40180799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201230960	chr12:40180799-40180800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573159113	chr12:40180814-40180815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183311886	chr12:40180822-40180823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559807471	chr12:40180864-40180865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187576141	chr12:40180892-40180893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139472255	chr12:40180900-40180901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114743431	chr12:40180963-40180964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191906215	chr12:40181022-40181023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551861144	chr12:40181188-40181189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183010494	chr12:40181220-40181221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186784019	chr12:40181247-40181248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375847806	chr12:40181254-40181255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559568911	chr12:40181266-40181267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561392689	chr12:40181275-40181276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537882448	chr12:40181283-40181284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6581338	chr12:40181334-40181335	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs36115078	chr12:40181337-40181338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149961418	chr12:40181341-40181342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530782239	chr12:40181366-40181367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189657486	chr12:40181393-40181394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567453863	chr12:40181433-40181434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73102575	chr12:40181496-40181497	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs554265167	chr12:40181505-40181506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546837257	chr12:40181506-40181507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571738589	chr12:40181560-40181561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144109042	chr12:40181609-40181610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182707822	chr12:40181625-40181626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557325625	chr12:40181696-40181697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527807464	chr12:40181698-40181699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569655852	chr12:40181712-40181713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs9645805	chr12:40181778-40181779	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs555389828	chr12:40181820-40181821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573812360	chr12:40181834-40181835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148671115	chr12:40181872-40181873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs117133140	chr12:40181948-40181949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187067295	chr12:40181955-40181956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs193184085	chr12:40182015-40182016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	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
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40158200-40199000	Weak transcription	Left Ventricle	heart
2	chr12:40161600-40198800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr12:40174400-40186200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr12:40176200-40189400	Weak transcription	Colon Smooth Muscle	Colon
5	chr12:40179800-40180600	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr12:40180200-40180600	Enhancers	HSMMtube	muscle
7	chr12:40180600-40189200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr12:40186200-40186800	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr12:40186400-40186600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr12:40186800-40187400	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr12:40187400-40187600	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr12:40188600-40188800	Enhancers	Rectal Smooth Muscle	rectum
13	chr12:40188800-40193400	Weak transcription	Rectal Smooth Muscle	rectum
14	chr12:40189200-40189800	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr12:40189400-40189600	Enhancers	Colon Smooth Muscle	Colon
16	chr12:40189600-40190000	Weak transcription	Colon Smooth Muscle	Colon
17	chr12:40190000-40190800	Enhancers	Colon Smooth Muscle	Colon
18	chr12:40190800-40197600	Weak transcription	Colon Smooth Muscle	Colon
19	chr12:40191600-40194200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr12:40193400-40193600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr12:40193400-40193800	Enhancers	Rectal Smooth Muscle	rectum
22	chr12:40193600-40193800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr12:40193600-40193800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr12:40193800-40198400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr12:40193800-40255800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr12:40194000-40198400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr12:40194600-40232600	Weak transcription	Right Ventricle	heart
28	chr12:40195600-40196000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:40197400-40197600	Enhancers	Liver	Liver
30	chr12:40197600-40198200	Weak transcription	Liver	Liver
31	chr12:40197600-40198800	Enhancers	Colon Smooth Muscle	Colon
32	chr12:40198200-40200600	Enhancers	Liver	Liver
33	chr12:40198400-40199200	Enhancers	Rectal Smooth Muscle	rectum
34	chr12:40198400-40200000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr12:40198600-40199000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr12:40198600-40199200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr12:40198800-40199200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr12:40198800-40199200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr12:40198800-40199200	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr12:40198800-40200000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr12:40199000-40199200	Enhancers	Left Ventricle	heart
42	chr12:40199000-40199800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:40199200-40199800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr12:40199200-40199800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr12:40199200-40200000	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr12:40199200-40265400	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr12:40199400-40199800	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr12:40199800-40200000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:40200000-40205000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:40200000-40205800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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