Variant report

Variant	nsv875208
Chromosome Location	chr2:141657878-141795620
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	chr2:141786570-141786643	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:141787024-141787341	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr2:141663058-141663247	H1-hESC	embryonic stem cell:	n/a	n/a
4	CCNT2	chr2:141680605-141680805	K562	blood:	n/a	n/a
5	CEBPB	chr2:141787064-141787627	H1-hESC	embryonic stem cell:	n/a	chr2:141787451-141787462
6	CEBPB	chr2:141755586-141755934	Hela-S3	cervix:	n/a	chr2:141755748-141755761 chr2:141755749-141755760 chr2:141755748-141755761 chr2:141755748-141755759 chr2:141755750-141755759 chr2:141755750-141755759 chr2:141755750-141755759 chr2:141755750-141755759
7	CEBPB	chr2:141662921-141663362	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr2:141787270-141787646	HepG2	liver:	n/a	chr2:141787451-141787462
9	CEBPB	chr2:141787364-141787503	HepG2	liver:	n/a	chr2:141787451-141787462
10	CEBPB	chr2:141710353-141710587	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:141755615-141755895	A549	lung:	n/a	chr2:141755748-141755761 chr2:141755749-141755760 chr2:141755748-141755761 chr2:141755748-141755759 chr2:141755750-141755759 chr2:141755750-141755759 chr2:141755750-141755759 chr2:141755750-141755759
12	CEBPB	chr2:141748148-141748484	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr2:141678158-141678292	A549	lung:	n/a	chr2:141678229-141678240 chr2:141678230-141678241 chr2:141678231-141678240
14	CEBPB	chr2:141732860-141733107	HepG2	liver:	n/a	chr2:141732951-141732962 chr2:141732950-141732963 chr2:141732950-141732961
15	CEBPB	chr2:141732771-141733140	IMR90	lung:	n/a	chr2:141732951-141732962 chr2:141732950-141732963 chr2:141732950-141732961
16	CEBPB	chr2:141755585-141755929	HepG2	liver:	n/a	chr2:141755748-141755761 chr2:141755749-141755760 chr2:141755748-141755761 chr2:141755748-141755759 chr2:141755750-141755759 chr2:141755750-141755759 chr2:141755750-141755759 chr2:141755750-141755759
17	CEBPB	chr2:141748038-141748534	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:141787284-141787628	A549	lung:	n/a	chr2:141787451-141787462
19	CEBPB	chr2:141746174-141746463	Hela-S3	cervix:	n/a	chr2:141746296-141746307
20	CEBPB	chr2:141787267-141787636	IMR90	lung:	n/a	chr2:141787451-141787462
21	CEBPB	chr2:141678081-141678357	HepG2	liver:	n/a	chr2:141678229-141678240 chr2:141678230-141678241 chr2:141678231-141678240
22	CEBPB	chr2:141678105-141678376	IMR90	lung:	n/a	chr2:141678229-141678240 chr2:141678230-141678241 chr2:141678231-141678240
23	CEBPB	chr2:141732791-141733123	Hela-S3	cervix:	n/a	chr2:141732951-141732962 chr2:141732950-141732963 chr2:141732950-141732961
24	CEBPB	chr2:141755574-141755952	IMR90	lung:	n/a	chr2:141755748-141755761 chr2:141755749-141755760 chr2:141755748-141755761 chr2:141755748-141755759 chr2:141755750-141755759 chr2:141755750-141755759 chr2:141755750-141755759 chr2:141755750-141755759
25	CEBPB	chr2:141699338-141699535	HepG2	liver:	n/a	n/a
26	CTCF	chr2:141701560-141701710	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr2:141722020-141722170	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr2:141721940-141722090	GM12867	blood:	n/a	n/a
29	CTCF	chr2:141701500-141701650	GM12875	blood:	n/a	n/a
30	CTCF	chr2:141701580-141701730	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr2:141721897-141722320	K562	blood:	n/a	n/a
32	CTCF	chr2:141722033-141722173	IMR90	lung:	n/a	n/a
33	CTCF	chr2:141722020-141722170	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr2:141722000-141722150	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr2:141722003-141722198	NHEK	skin:	n/a	n/a
36	CTCF	chr2:141722020-141722170	HepG2	liver:	n/a	n/a
37	CTCF	chr2:141722040-141722190	AG04449	skin:	n/a	n/a
38	CTCF	chr2:141721940-141722090	GM12869	blood:	n/a	n/a
39	CTCF	chr2:141701360-141701510	HAc	cerebellar:	n/a	n/a
40	CTCF	chr2:141750460-141750610	HMF	breast:	n/a	n/a
41	CTCF	chr2:141722000-141722150	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr2:141722060-141722210	RPTEC	kidney:	n/a	n/a
43	CTCF	chr2:141722020-141722170	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr2:141722000-141722150	HMEC	breast:	n/a	n/a
45	CTCF	chr2:141722000-141722150	GM12878	blood:	n/a	n/a
46	CTCF	chr2:141701540-141701690	GM12872	blood:	n/a	n/a
47	CTCF	chr2:141722078-141722182	GM19239	blood:	n/a	n/a
48	CTCF	chr2:141722018-141722250	K562	blood:	n/a	n/a
49	CTCF	chr2:141722040-141722190	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr2:141721979-141722218	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:141787134-141787184	Caco-2	colon:	n/a
2	chr2:141751626-141751676	AG09319	gingival:	n/a
3	chr2:141751626-141751676	HRCEpiC	kidney:	n/a
4	chr2:141755389-141755439	Caco-2	colon:	n/a
5	chr2:141787134-141787184	GM12892	blood:	n/a
6	chr2:141662876-141662926	HL-60	blood:	n/a
7	chr2:141795320-141795370	ECC-1	luminal epithelium:	n/a
8	chr2:141795320-141795370	HUVEC	blood vessel:	n/a
9	chr2:141751626-141751676	HCT-116	colon:	n/a
10	chr2:141755389-141755439	GM12891	blood:	n/a
11	chr2:141751626-141751676	SK-N-MC	brain:	n/a
12	chr2:141795320-141795370	PFSK-1	brain:	n/a
13	chr2:141755389-141755439	LNCaP	prostate:	n/a
14	chr2:141795320-141795370	NH-A	brain:	n/a
15	chr2:141795320-141795370	GM12891	blood:	n/a
16	chr2:141795320-141795370	GM06990	blood:	n/a
17	chr2:141795320-141795370	HMEC	breast:	n/a
18	chr2:141751626-141751676	SK-N-SH	brain:	n/a
19	chr2:141662876-141662926	SK-N-SH_RA	brain:	n/a
20	chr2:141751626-141751676	HCM	heart:	n/a
21	chr2:141795320-141795370	GM19239	blood:	n/a
22	chr2:141662876-141662926	AG04449	skin:	fetal
23	chr2:141795320-141795370	A549	lung:	n/a
24	chr2:141787134-141787184	GM12878	blood:	n/a
25	chr2:141662876-141662926	T-47D	breast:	n/a
26	chr2:141662876-141662926	HEEpiC	esophagus:	n/a
27	chr2:141787134-141787184	U87	brain:	n/a
28	chr2:141662876-141662926	AoSMC	blood vessel:	n/a
29	chr2:141787134-141787184	AG10803	skin:	n/a
30	chr2:141795320-141795370	NT2-D1	testis:	n/a
31	chr2:141795320-141795370	Jurkat	blood:	n/a
32	chr2:141755389-141755439	AG04450	lung:	fetal
33	chr2:141795320-141795370	PANC-1	pancreas:	n/a
34	chr2:141787134-141787184	CMK	blood:	n/a
35	chr2:141751626-141751676	Hepatocyte	liver:	n/a
36	chr2:141787134-141787184	PANC-1	pancreas:	n/a
37	chr2:141787134-141787184	HCT-116	colon:	n/a
38	chr2:141787134-141787184	K562	blood:	n/a
39	chr2:141755389-141755439	Hela-S3	cervix:	n/a
40	chr2:141751626-141751676	U87	brain:	n/a
41	chr2:141755389-141755439	GM06990	blood:	n/a
42	chr2:141662876-141662926	SAEC	small airway:	n/a
43	chr2:141787134-141787184	PrEC	prostate:	n/a
44	chr2:141751626-141751676	HepG2	liver:	n/a
45	chr2:141755389-141755439	AG09319	gingival:	n/a
46	chr2:141755389-141755439	HEK293	kidney:	embryo
47	chr2:141795320-141795370	HCF	heart:	n/a
48	chr2:141795320-141795370	SK-N-SH	brain:	n/a
49	chr2:141787134-141787184	HPAEpiC	pulmonary alveolar:	n/a
50	chr2:141787134-141787184	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:141691853..141693372-chr2:141697012..141698954,2	MCF-7	breast:
2	chr2:141736437..141738156-chr2:141740284..141742486,2	MCF-7	breast:
3	chr2:141747914..141749920-chr2:141751222..141752876,2	MCF-7	breast:
4	chr2:141736437..141738156-chr2:141740284..141742486,2	MCF-7	breast:
5	chr2:141691853..141693372-chr2:141697012..141698954,2	MCF-7	breast:
6	chr2:141747914..141749920-chr2:141751222..141752876,2	MCF-7	breast:
7	chr2:141785789..141788273-chr2:141812722..141815557,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000201892	TF binding region
ENSG00000201892	CpG island

Extended variants
information (count: 3371 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3371 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2033290	chr2:141657878-141657879	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549418265	chr2:141657889-141657890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569299014	chr2:141657909-141657910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116075361	chr2:141657916-141657917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551889576	chr2:141657965-141657966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs72990131	chr2:141658004-141658005	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs73964740	chr2:141658041-141658042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs139649795	chr2:141658072-141658073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567575483	chr2:141658183-141658184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181021440	chr2:141658274-141658275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73964742	chr2:141658330-141658331	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs1366804	chr2:141658368-141658369	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs367988479	chr2:141658381-141658382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372090329	chr2:141658382-141658383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs397753706	chr2:141658388-141658389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79870140	chr2:141658452-141658453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558621186	chr2:141658478-141658479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs578080604	chr2:141658502-141658503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540837157	chr2:141658507-141658508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560592987	chr2:141658525-141658526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529587050	chr2:141658548-141658549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185911924	chr2:141658587-141658588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530848085	chr2:141658591-141658592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531742181	chr2:141658598-141658599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570619632	chr2:141658639-141658640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571731820	chr2:141658656-141658657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145213384	chr2:141658713-141658714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561052502	chr2:141658719-141658720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191065183	chr2:141658754-141658755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183264175	chr2:141658757-141658758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112784063	chr2:141658764-141658765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146925053	chr2:141658766-141658767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536133875	chr2:141658814-141658815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556086887	chr2:141658951-141658952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569262188	chr2:141658970-141658971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148720643	chr2:141659000-141659001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142441291	chr2:141659011-141659012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186105286	chr2:141659088-141659089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190574315	chr2:141659090-141659091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4954862	chr2:141659095-141659096	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs574323420	chr2:141659117-141659118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543338913	chr2:141659147-141659148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539298314	chr2:141659223-141659224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563187283	chr2:141659236-141659237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576473673	chr2:141659247-141659248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376179019	chr2:141659274-141659275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183326559	chr2:141659281-141659282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114253261	chr2:141659286-141659287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188378495	chr2:141659289-141659290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367607678	chr2:141659299-141659300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	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
Bipolar disorder	19114987	CNVD
Esophageal cancer	21851588	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141649200-141661800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr2:141653600-141662800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr2:141655000-141658600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:141658800-141659000	Enhancers	Brain Anterior Caudate	brain
5	chr2:141658800-141659200	Enhancers	Brain Substantia Nigra	brain
6	chr2:141659000-141659400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:141659400-141659600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:141659600-141659800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:141659800-141660600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:141660600-141661800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:141661800-141662200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:141662200-141662600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:141662200-141662800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr2:141662200-141663400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr2:141662200-141663600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr2:141662200-141663800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
17	chr2:141662400-141662800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr2:141662400-141662800	Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr2:141662400-141663200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr2:141662400-141663800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr2:141662600-141663800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr2:141662600-141663800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:141662800-141663000	Enhancers	H9 Cell Line	embryonic stem cell
24	chr2:141662800-141663000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr2:141662800-141663200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr2:141662800-141663200	Enhancers	Fetal Heart	heart
27	chr2:141662800-141663400	Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr2:141662800-141663400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr2:141662800-141663400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr2:141663000-141663800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr2:141663200-141663400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
32	chr2:141663200-141663800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr2:141663200-141668200	Weak transcription	Fetal Heart	heart
34	chr2:141663400-141663800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
35	chr2:141663600-141663800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
36	chr2:141663800-141664000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
37	chr2:141663800-141664600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:141664600-141665400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:141668200-141668600	Enhancers	Fetal Heart	heart
40	chr2:141673800-141674200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr2:141673800-141674600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr2:141677000-141677800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr2:141686000-141686800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr2:141686200-141686400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr2:141686400-141687400	Enhancers	Brain Germinal Matrix	brain
46	chr2:141686800-141691800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr2:141687200-141687800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr2:141687200-141687800	Enhancers	Fetal Lung	lung
49	chr2:141687400-141687800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr2:141687400-141687800	Enhancers	Adipose Nuclei	Adipose

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