Variant report

Variant	nsv459663
Chromosome Location	chr2:142509570-142568465
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	BACH1	chr2:142530297-142530358	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr2:142556827-142557091	GM12878	blood:	n/a	n/a
3	CEBPB	chr2:142549134-142549357	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr2:142564329-142564530	HepG2	liver:	n/a	chr2:142564423-142564436 chr2:142564423-142564434
5	CEBPB	chr2:142516782-142516903	A549	lung:	n/a	n/a
6	CEBPB	chr2:142522920-142523155	H1-hESC	embryonic stem cell:	n/a	chr2:142523034-142523047 chr2:142523036-142523047
7	CEBPB	chr2:142527770-142527964	HepG2	liver:	n/a	chr2:142527873-142527882 chr2:142527873-142527884
8	CEBPB	chr2:142549080-142549369	HepG2	liver:	n/a	chr2:142549089-142549101
9	CEBPB	chr2:142533978-142534245	HepG2	liver:	n/a	chr2:142534106-142534117
10	CEBPB	chr2:142549199-142549267	A549	lung:	n/a	n/a
11	CTCF	chr2:142549353-142549358	LNCaP	prostate:	n/a	n/a
12	CTCF	chr2:142514551-142514588	K562	blood:	n/a	n/a
13	CTCF	chr2:142549302-142549350	LNCaP	prostate:	n/a	n/a
14	CTCF	chr2:142528268-142528311	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr2:142528158-142528386	H1-hESC	embryonic stem cell:	n/a	n/a
16	E2F4	chr2:142523805-142523854	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr2:142521361-142521544	MCF10A-Er-Src	breast:	n/a	n/a
18	EBF1	chr2:142555247-142555282	GM12878	blood:	n/a	n/a
19	EP300	chr2:142524651-142524962	SK-N-SH	brain:	n/a	chr2:142524708-142524718
20	EP300	chr2:142513708-142513790	GM12878	blood:	n/a	n/a
21	EP300	chr2:142556839-142557090	GM12878	blood:	n/a	n/a
22	FAM48A	chr2:142523936-142524136	GM12878	blood:	n/a	n/a
23	FOS	chr2:142524808-142525032	MCF10A-Er-Src	breast:	n/a	chr2:142524859-142524871 chr2:142524860-142524870 chr2:142524861-142524870 chr2:142524859-142524866
24	FOS	chr2:142542107-142542300	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr2:142524706-142524990	MCF10A-Er-Src	breast:	n/a	chr2:142524859-142524871 chr2:142524860-142524870 chr2:142524861-142524870 chr2:142524859-142524866
26	FOS	chr2:142524642-142525027	MCF10A-Er-Src	breast:	n/a	chr2:142524859-142524871 chr2:142524860-142524870 chr2:142524861-142524870 chr2:142524859-142524866
27	FOS	chr2:142524688-142525017	MCF10A-Er-Src	breast:	n/a	chr2:142524859-142524871 chr2:142524860-142524870 chr2:142524861-142524870 chr2:142524859-142524866
28	FOSL2	chr2:142524569-142525117	SK-N-SH	brain:	n/a	chr2:142524859-142524871 chr2:142524860-142524870 chr2:142524861-142524870 chr2:142524859-142524866
29	FOXM1	chr2:142556743-142557066	GM12878	blood:	n/a	n/a
30	GATA3	chr2:142524628-142525008	SK-N-SH	brain:	n/a	chr2:142524859-142524868
31	GATA3	chr2:142524610-142525038	SK-N-SH	brain:	n/a	chr2:142524859-142524868
32	IRF3	chr2:142560418-142560430	GM12878	blood:	n/a	n/a
33	JUN	chr2:142518304-142518370	H1-hESC	embryonic stem cell:	n/a	n/a
34	JUND	chr2:142524582-142525011	SK-N-SH	brain:	n/a	chr2:142524859-142524870 chr2:142524859-142524871 chr2:142524860-142524870 chr2:142524861-142524870 chr2:142524859-142524866
35	JUND	chr2:142524705-142525043	HepG2	liver:	n/a	chr2:142524859-142524870 chr2:142524859-142524871 chr2:142524860-142524870 chr2:142524861-142524870 chr2:142524859-142524866
36	JUND	chr2:142563435-142563660	HepG2	liver:	n/a	chr2:142563497-142563508 chr2:142563500-142563507 chr2:142563498-142563508 chr2:142563497-142563509 chr2:142563499-142563507 chr2:142563499-142563508
37	MAFF	chr2:142554068-142554318	K562	blood:	n/a	chr2:142554201-142554219 chr2:142554200-142554214
38	MAFF	chr2:142540161-142540517	HepG2	liver:	n/a	n/a
39	MAFF	chr2:142554060-142554381	HepG2	liver:	n/a	chr2:142554201-142554219 chr2:142554200-142554214
40	MAFF	chr2:142540216-142540482	K562	blood:	n/a	n/a
41	MAFK	chr2:142554063-142554378	IMR90	lung:	n/a	chr2:142554197-142554217 chr2:142554199-142554215 chr2:142554201-142554211 chr2:142554200-142554214 chr2:142554202-142554217
42	MAFK	chr2:142542756-142542796	HepG2	liver:	n/a	n/a
43	MAFK	chr2:142554084-142554370	K562	blood:	n/a	chr2:142554197-142554217 chr2:142554199-142554215 chr2:142554201-142554211 chr2:142554200-142554214 chr2:142554202-142554217
44	MAFK	chr2:142540186-142540474	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAFK	chr2:142524792-142524966	IMR90	lung:	n/a	chr2:142524887-142524904 chr2:142524863-142524877
46	MAFK	chr2:142554031-142554387	HepG2	liver:	n/a	chr2:142554197-142554217 chr2:142554199-142554215 chr2:142554201-142554211 chr2:142554200-142554214 chr2:142554202-142554217
47	MAFK	chr2:142566861-142567022	HepG2	liver:	n/a	chr2:142566999-142567014
48	MAFK	chr2:142554045-142554380	HepG2	liver:	n/a	chr2:142554197-142554217 chr2:142554199-142554215 chr2:142554201-142554211 chr2:142554200-142554214 chr2:142554202-142554217
49	MAFK	chr2:142554103-142554371	H1-hESC	embryonic stem cell:	n/a	chr2:142554197-142554217 chr2:142554199-142554215 chr2:142554201-142554211 chr2:142554200-142554214 chr2:142554202-142554217
50	MAFK	chr2:142566894-142567084	HepG2	liver:	n/a	chr2:142566999-142567014

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:142530447-142530497	T-47D	breast:	n/a
2	chr2:142530447-142530497	AG09319	gingival:	n/a
3	chr2:142530447-142530497	HCPEpiC	choroid plexus:	n/a
4	chr2:142530447-142530497	AG09309	skin:	n/a
5	chr2:142530447-142530497	GM06990	blood:	n/a
6	chr2:142530447-142530497	HNPCEpiC	eye:	n/a
7	chr2:142530447-142530497	RPTEC	kidney:	n/a
8	chr2:142530447-142530497	PFSK-1	brain:	n/a
9	chr2:142530447-142530497	HEEpiC	esophagus:	n/a
10	chr2:142530447-142530497	AG04449	skin:	fetal
11	chr2:142530447-142530497	HEK293	kidney:	embryo
12	chr2:142530447-142530497	SK-N-SH_RA	brain:	n/a
13	chr2:142530447-142530497	SAEC	small airway:	n/a
14	chr2:142530447-142530497	CMK	blood:	n/a
15	chr2:142530447-142530497	PrEC	prostate:	n/a
16	chr2:142530447-142530497	HAEpiC	amniotic membrane:	n/a
17	chr2:142530447-142530497	NH-A	brain:	n/a
18	chr2:142530447-142530497	HepG2	liver:	n/a
19	chr2:142530447-142530497	GM12878	blood:	n/a
20	chr2:142530447-142530497	NB4	blood:	n/a
21	chr2:142530447-142530497	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:142530447-142530497	HCT-116	colon:	n/a
23	chr2:142530447-142530497	NHBE	bronchial:	n/a
24	chr2:142530447-142530497	GM12892	blood:	n/a
25	chr2:142530447-142530497	HRE	kidney:	n/a
26	chr2:142530447-142530497	HRPEpiC	eye:	n/a
27	chr2:142530447-142530497	H1-hESC	embryonic stem cell:	embryo
28	chr2:142530447-142530497	ECC-1	luminal epithelium:	n/a
29	chr2:142530447-142530497	SK-N-MC	brain:	n/a
30	chr2:142530447-142530497	SKMC	muscle:	n/a
31	chr2:142530447-142530497	ProgFib	skin:	n/a
32	chr2:142530447-142530497	GM19239	blood:	n/a
33	chr2:142530447-142530497	AG04450	lung:	fetal
34	chr2:142530447-142530497	PANC-1	pancreas:	n/a
35	chr2:142530447-142530497	HIPEpiC	eye:	n/a
36	chr2:142530447-142530497	NHDF-neo	bronchial:	n/a
37	chr2:142530447-142530497	AoSMC	blood vessel:	n/a
38	chr2:142530447-142530497	A549	lung:	n/a
39	chr2:142530447-142530497	Caco-2	colon:	n/a
40	chr2:142530447-142530497	MCF-7	breast:	n/a
41	chr2:142530447-142530497	LNCaP	prostate:	n/a
42	chr2:142530447-142530497	HRCEpiC	kidney:	n/a
43	chr2:142530447-142530497	HUVEC	blood vessel:	n/a
44	chr2:142530447-142530497	HCM	heart:	n/a
45	chr2:142530447-142530497	NT2-D1	testis:	n/a
46	chr2:142530447-142530497	Hepatocyte	liver:	n/a
47	chr2:142530447-142530497	HMEC	breast:	n/a
48	chr2:142530447-142530497	GM12891	blood:	n/a
49	chr2:142530447-142530497	Hela-S3	cervix:	n/a
50	chr2:142530447-142530497	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:142519003..142520660-chr2:142522253..142524916,2	K562	blood:
2	chr2:142532703..142535665-chr2:142536672..142538561,2	MCF-7	breast:
3	chr2:142519003..142520660-chr2:142522253..142524916,2	K562	blood:
4	chr2:142507099..142509499-chr2:142523507..142526473,2	MCF-7	breast:
5	chr2:142538922..142540737-chr2:142542566..142546321,3	MCF-7	breast:
6	chr2:142538922..142540737-chr2:142542566..142546321,3	MCF-7	breast:
7	chr2:142536364..142538824-chr2:142574055..142576511,2	K562	blood:
8	chr2:142532703..142535665-chr2:142536672..142538561,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTDC1-26	chr2:142562933-142563323	NONHSAT074708
2	lnc-GTDC1-26	chr2:142567848-142567970	NONHSAT074708

Variant related genes	Relation type
LRP1B	TF binding region
LRP1B	CpG island

Extended variants
information (count: 817 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16847075	chr2:142519811-142519812	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543991731	chr2:142519819-142519820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs62168693	chr2:142519839-142519840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141103332	chr2:142519877-142519878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs72847471	chr2:142519976-142519977	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs113020568	chr2:142520024-142520025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552665069	chr2:142520093-142520094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs72847474	chr2:142520123-142520124	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs535955765	chr2:142520124-142520125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554656517	chr2:142520139-142520140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575582836	chr2:142520142-142520143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552835375	chr2:142520168-142520169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567970334	chr2:142520174-142520175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116735999	chr2:142520205-142520206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149839612	chr2:142520268-142520269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546654253	chr2:142520269-142520270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570361443	chr2:142520297-142520298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565203072	chr2:142520303-142520304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539125974	chr2:142520310-142520311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs553067514	chr2:142520316-142520317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552207583	chr2:142520321-142520322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568132628	chr2:142520322-142520323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572868028	chr2:142520339-142520340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs202057879	chr2:142520388-142520389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555076467	chr2:142520394-142520395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575200281	chr2:142520406-142520407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544173900	chr2:142520419-142520420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75277514	chr2:142520428-142520429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61666362	chr2:142520432-142520433	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs373385257	chr2:142520442-142520443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559767282	chr2:142520496-142520497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141797456	chr2:142520550-142520551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180803552	chr2:142520551-142520552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559685387	chr2:142520568-142520569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561788494	chr2:142520581-142520582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79500165	chr2:142520583-142520584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185183609	chr2:142520652-142520653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190081570	chr2:142520654-142520655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533116057	chr2:142520662-142520663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546481129	chr2:142520677-142520678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147084963	chr2:142520752-142520753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538098903	chr2:142520789-142520790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535236711	chr2:142520830-142520831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555398091	chr2:142520856-142520857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541911915	chr2:142520891-142520892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147806073	chr2:142520906-142520907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537721931	chr2:142520919-142520920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6711195	chr2:142520965-142520966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148842369	chr2:142520988-142520989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370632543	chr2:142521015-142521016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma	21080181	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Autism	22543975	CNVD
Cancer	20164920	CNVD
Hypertension	22686481	CNVD
Hypospadia	22686481	CNVD
Intellectual disability	22686481	CNVD
Omphalocele	22686481	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142519800-142520400	Enhancers	Dnd41	blood
2	chr2:142520400-142523200	Weak transcription	Dnd41	blood
3	chr2:142523200-142524800	Enhancers	Dnd41	blood
4	chr2:142524000-142524800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr2:142524000-142525000	Enhancers	Brain Cingulate Gyrus	brain
6	chr2:142524000-142525400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr2:142524000-142525800	Enhancers	NH-A	brain
8	chr2:142524200-142524400	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr2:142524200-142524800	Enhancers	Muscle Satellite Cultured Cells	--
10	chr2:142524200-142524800	Enhancers	Brain Hippocampus Middle	brain
11	chr2:142524400-142525800	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr2:142524600-142525000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr2:142524600-142526200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr2:142524800-142525000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr2:142524800-142525600	Enhancers	Brain Substantia Nigra	brain
16	chr2:142525000-142525200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr2:142525000-142525400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr2:142525000-142527200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr2:142525000-142530200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr2:142525200-142525600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:142525200-142525800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr2:142525200-142526800	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr2:142525400-142527200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr2:142525400-142528000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr2:142526200-142527200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:142526800-142527000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr2:142527000-142527400	Enhancers	H9 Cell Line	embryonic stem cell
28	chr2:142527000-142527800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr2:142527200-142528400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr2:142527200-142528400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr2:142527200-142528600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr2:142527200-142528600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr2:142527400-142530200	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr2:142527800-142528200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr2:142528000-142528400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr2:142528200-142530200	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr2:142528400-142530200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr2:142528400-142530200	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr2:142528400-142530200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr2:142528600-142530200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr2:142530200-142530400	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr2:142530200-142530600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr2:142530200-142530800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr2:142530200-142531200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr2:142530200-142531400	Enhancers	H9 Cell Line	embryonic stem cell
46	chr2:142530200-142531400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr2:142530200-142531600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr2:142530400-142530800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr2:142530800-142531200	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr2:142535600-142536000	Enhancers	Dnd41	blood

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