Variant report

Variant	nsv997699
Chromosome Location	chr2:188052351-188142073
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:264)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188082673-188083042	K562	blood:	n/a	chr2:188082805-188082821 chr2:188082806-188082822
2	ATF2	chr2:188128538-188128835	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr2:188075532-188075733	K562	blood:	n/a	n/a
4	BATF	chr2:188092264-188092475	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:188089782-188090028	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr2:188075474-188075737	K562	blood:	n/a	chr2:188075578-188075589
7	CEBPB	chr2:188075456-188075728	HepG2	liver:	n/a	chr2:188075578-188075589
8	CEBPB	chr2:188061256-188061303	K562	blood:	n/a	n/a
9	CEBPB	chr2:188128014-188128379	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr2:188064139-188064438	HepG2	liver:	n/a	chr2:188064300-188064311 chr2:188064301-188064312
11	CEBPB	chr2:188075435-188075790	HepG2	liver:	n/a	chr2:188075578-188075589
12	CEBPB	chr2:188064188-188064450	K562	blood:	n/a	chr2:188064300-188064311 chr2:188064301-188064312
13	CEBPB	chr2:188075525-188075712	K562	blood:	n/a	chr2:188075578-188075589
14	CEBPB	chr2:188128072-188128355	IMR90	lung:	n/a	n/a
15	CEBPB	chr2:188092236-188092364	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:188075457-188075812	Hela-S3	cervix:	n/a	chr2:188075578-188075589
17	CEBPB	chr2:188092236-188092435	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr2:188107016-188107020	IMR90	lung:	n/a	n/a
19	CHD2	chr2:188089735-188090140	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr2:188073313-188073360	HepG2	liver:	n/a	n/a
21	CREB1	chr2:188089728-188090143	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr2:188136640-188136790	Caco-2	colon:	n/a	n/a
23	CTCF	chr2:188136740-188136890	GM06990	blood:	n/a	n/a
24	CTCF	chr2:188136640-188136790	GM12873	blood:	n/a	n/a
25	CTCF	chr2:188136620-188136770	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr2:188070449-188070488	GM20000	blood:	n/a	n/a
27	CTCF	chr2:188059820-188059970	HMF	breast:	n/a	chr2:188059882-188059903 chr2:188059881-188059897 chr2:188059885-188059893
28	CTCF	chr2:188125483-188125545	GM10248	blood:	n/a	n/a
29	CTCF	chr2:188120802-188120876	Fibrobl	skin:	n/a	n/a
30	CTCF	chr2:188073260-188073410	HepG2	liver:	n/a	n/a
31	CTCF	chr2:188125400-188125509	LNCaP	prostate:	n/a	n/a
32	CTCF	chr2:188136720-188136870	HMEC	breast:	n/a	n/a
33	CTCF	chr2:188067099-188067116	Fibrobl	skin:	n/a	n/a
34	CTCF	chr2:188136755-188136832	HepG2	liver:	n/a	n/a
35	CTCF	chr2:188059780-188059930	HCPEpiC	choroid plexus:	n/a	chr2:188059882-188059903 chr2:188059881-188059897 chr2:188059885-188059893
36	CTCF	chr2:188136727-188136805	GM12878	blood:	n/a	n/a
37	CTCF	chr2:188059840-188059990	HCPEpiC	choroid plexus:	n/a	chr2:188059882-188059903 chr2:188059881-188059897 chr2:188059885-188059893
38	CTCF	chr2:188136680-188136830	HMEC	breast:	n/a	n/a
39	CTCF	chr2:188136750-188136786	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr2:188136660-188136810	GM12875	blood:	n/a	n/a
41	CTCF	chr2:188059860-188060010	RPTEC	kidney:	n/a	chr2:188059882-188059903 chr2:188059881-188059897 chr2:188059885-188059893
42	CTCF	chr2:188075340-188075490	HepG2	liver:	n/a	n/a
43	CTCF	chr2:188136680-188136830	GM12864	blood:	n/a	n/a
44	CTCF	chr2:188132300-188132450	GM12869	blood:	n/a	n/a
45	CTCF	chr2:188136700-188136850	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr2:188125440-188125474	Lung_OC	lung:	n/a	n/a
47	CTCF	chr2:188136723-188136797	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:188073279-188073409	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr2:188073360-188073510	GM12867	blood:	n/a	n/a
50	CTCF	chr2:188136657-188136930	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188093537-188093587	SK-N-SH_RA	brain:	n/a
2	chr2:188093537-188093587	LNCaP	prostate:	n/a
3	chr2:188128809-188128859	IMR90	lung:	fetal
4	chr2:188093537-188093587	HRCEpiC	kidney:	n/a
5	chr2:188093537-188093587	HPAEpiC	pulmonary alveolar:	n/a
6	chr2:188128809-188128859	HCPEpiC	choroid plexus:	n/a
7	chr2:188128809-188128859	SKMC	muscle:	n/a
8	chr2:188093537-188093587	GM19239	blood:	n/a
9	chr2:188128809-188128859	HL-60	blood:	n/a
10	chr2:188128809-188128859	AG04449	skin:	fetal
11	chr2:188093537-188093587	BJ	skin:	n/a
12	chr2:188093537-188093587	HCM	heart:	n/a
13	chr2:188093537-188093587	BE2_C	brain:	n/a
14	chr2:188128809-188128859	HCF	heart:	n/a
15	chr2:188093537-188093587	NHBE	bronchial:	n/a
16	chr2:188128809-188128859	Caco-2	colon:	n/a
17	chr2:188128809-188128859	GM19239	blood:	n/a
18	chr2:188128809-188128859	AG04450	lung:	fetal
19	chr2:188093537-188093587	Hela-S3	cervix:	n/a
20	chr2:188128809-188128859	NT2-D1	testis:	n/a
21	chr2:188128809-188128859	HEK293	kidney:	embryo
22	chr2:188128809-188128859	GM12891	blood:	n/a
23	chr2:188093537-188093587	HNPCEpiC	eye:	n/a
24	chr2:188128809-188128859	HMEC	breast:	n/a
25	chr2:188093537-188093587	NH-A	brain:	n/a
26	chr2:188128809-188128859	HCT-116	colon:	n/a
27	chr2:188093537-188093587	MCF10A-Er-Src	breast:	n/a
28	chr2:188128809-188128859	BE2_C	brain:	n/a
29	chr2:188128809-188128859	AoSMC	blood vessel:	n/a
30	chr2:188128809-188128859	HUVEC	blood vessel:	n/a
31	chr2:188128809-188128859	A549	lung:	n/a
32	chr2:188128809-188128859	K562	blood:	n/a
33	chr2:188128809-188128859	U87	brain:	n/a
34	chr2:188093537-188093587	A549	lung:	n/a
35	chr2:188128809-188128859	HCM	heart:	n/a
36	chr2:188128809-188128859	MCF10A-Er-Src	breast:	n/a
37	chr2:188128809-188128859	SK-N-SH	brain:	n/a
38	chr2:188093537-188093587	HUVEC	blood vessel:	n/a
39	chr2:188093537-188093587	HRPEpiC	eye:	n/a
40	chr2:188093537-188093587	HEK293	kidney:	embryo
41	chr2:188093537-188093587	ECC-1	luminal epithelium:	n/a
42	chr2:188128809-188128859	MCF-7	breast:	n/a
43	chr2:188128809-188128859	GM06990	blood:	n/a
44	chr2:188093537-188093587	HCPEpiC	choroid plexus:	n/a
45	chr2:188128809-188128859	HAEpiC	amniotic membrane:	n/a
46	chr2:188128809-188128859	NH-A	brain:	n/a
47	chr2:188093537-188093587	AG09309	skin:	n/a
48	chr2:188093537-188093587	NHDF-neo	bronchial:	n/a
49	chr2:188093537-188093587	Jurkat	blood:	n/a
50	chr2:188093537-188093587	GM12878	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:188115424..188118005-chr2:188119188..188121188,2	MCF-7	breast:
2	chr2:188110055..188111838-chr2:188114697..188116780,2	K562	blood:
3	chr2:188081497..188084400-chr2:188085542..188087074,2	K562	blood:
4	chr2:188088219..188089827-chr2:188091606..188093417,2	K562	blood:
5	chr2:188049075..188051640-chr2:188058153..188060182,2	K562	blood:
6	chr2:188081497..188084400-chr2:188085542..188087074,2	K562	blood:
7	chr2:188118124..188120319-chr2:188121977..188123485,2	MCF-7	breast:
8	chr2:188082290..188085324-chr2:188088101..188090494,3	K562	blood:
9	chr2:188108987..188110844-chr2:188112727..188114579,2	K562	blood:
10	chr2:188088219..188089827-chr2:188091606..188093417,2	K562	blood:
11	chr2:188108987..188110844-chr2:188112727..188114579,2	K562	blood:
12	chr2:188082290..188085324-chr2:188088101..188090494,3	K562	blood:
13	chr2:188118124..188120319-chr2:188121977..188123485,2	MCF-7	breast:
14	chr2:188110055..188111838-chr2:188114697..188116780,2	K562	blood:
15	chr2:188115424..188118005-chr2:188119188..188121188,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM171B-1	chr2:188056562-188056658	NONHSAT076011
2	lnc-FAM171B-1	chr2:188060089-188060574	NONHSAT076011

No data

Variant related genes	Relation type
RNU6-989P	TF binding region
RNU6-989P	CpG island

Extended variants
information (count: 1397 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1397 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141213610	chr2:188052474-188052475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192979400	chr2:188052485-188052486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530629757	chr2:188052494-188052495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149895919	chr2:188052498-188052499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567244861	chr2:188052503-188052504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11894499	chr2:188052541-188052542	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs77607274	chr2:188052547-188052548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567271466	chr2:188052550-188052551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11894501	chr2:188052553-188052554	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs572011395	chr2:188052556-188052557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs72899302	chr2:188052589-188052590	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs571326926	chr2:188052661-188052662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs55941489	chr2:188052798-188052799	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs144958730	chr2:188052807-188052808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576840541	chr2:188052855-188052856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543630859	chr2:188053024-188053025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549535104	chr2:188053057-188053058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559150812	chr2:188053079-188053080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377640310	chr2:188053093-188053094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371319316	chr2:188053095-188053096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200297173	chr2:188053096-188053097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10523190	chr2:188053123-188053124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs71017379	chr2:188053140-188053141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116027874	chr2:188053156-188053157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35174644	chr2:188053159-188053160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34236360	chr2:188053161-188053162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541143890	chr2:188053194-188053195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559426933	chr2:188053260-188053261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4667151	chr2:188053293-188053294	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs541836873	chr2:188053348-188053349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183559355	chr2:188053408-188053409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560835204	chr2:188053529-188053530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188338349	chr2:188053589-188053590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549700348	chr2:188053775-188053776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181848338	chr2:188053824-188053825	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs532312793	chr2:188053927-188053928	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs547440889	chr2:188053940-188053941	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs373915875	chr2:188054001-188054002	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs565793454	chr2:188054005-188054006	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs115746069	chr2:188054007-188054008	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs114205453	chr2:188054016-188054017	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs570358255	chr2:188054057-188054058	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs537790808	chr2:188054066-188054067	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs541073139	chr2:188054106-188054107	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs558997744	chr2:188054129-188054130	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs577323723	chr2:188054164-188054165	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs149021535	chr2:188054177-188054178	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs186303345	chr2:188054197-188054198	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs575683093	chr2:188054233-188054234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs55833494	chr2:188054240-188054241	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188052200-188054600	Enhancers	HUVEC	blood vessel
2	chr2:188052200-188055600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:188052400-188053000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr2:188052600-188052800	Enhancers	Stomach Mucosa	stomach
5	chr2:188052800-188053400	Weak transcription	Stomach Mucosa	stomach
6	chr2:188053000-188053400	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr2:188053200-188055000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:188053400-188054200	Enhancers	Muscle Satellite Cultured Cells	--
9	chr2:188053400-188054200	Enhancers	Stomach Mucosa	stomach
10	chr2:188053600-188053800	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr2:188053600-188054200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr2:188053600-188054400	Enhancers	Rectal Mucosa Donor 29	rectum
13	chr2:188053800-188054000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
14	chr2:188053800-188054200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr2:188054000-188054200	Active TSS	Rectal Mucosa Donor 31	rectum
16	chr2:188054000-188054600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr2:188054200-188054600	Weak transcription	Stomach Mucosa	stomach
18	chr2:188054600-188055400	Enhancers	Stomach Mucosa	stomach
19	chr2:188062400-188063600	Enhancers	HUVEC	blood vessel
20	chr2:188070200-188071400	Enhancers	HUVEC	blood vessel
21	chr2:188070400-188071200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr2:188070600-188071200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr2:188070800-188071000	Enhancers	Adipose Nuclei	Adipose
24	chr2:188070800-188071200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:188072400-188073400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:188072800-188073400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:188074600-188074800	Enhancers	Fetal Intestine Small	intestine
28	chr2:188074800-188075000	Weak transcription	Fetal Intestine Small	intestine
29	chr2:188075000-188075600	ZNF genes & repeats	Fetal Intestine Small	intestine
30	chr2:188075200-188075400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr2:188075200-188075800	Enhancers	Fetal Intestine Large	intestine
32	chr2:188079400-188080200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr2:188080000-188081200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:188080000-188082000	Enhancers	HSMMtube	muscle
35	chr2:188080200-188080400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:188080200-188080600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr2:188080200-188080600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr2:188080200-188080600	Enhancers	HSMM	muscle
39	chr2:188080200-188080800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr2:188080200-188081000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:188080400-188080800	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr2:188080400-188080800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr2:188080400-188080800	Enhancers	Muscle Satellite Cultured Cells	--
44	chr2:188080400-188080800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr2:188080400-188081200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:188080400-188081400	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr2:188080400-188081600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr2:188080800-188083200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr2:188082200-188083200	Enhancers	K562	blood
50	chr2:188083200-188083400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain

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