Variant report

Variant	nsv1005875
Chromosome Location	chr2:168481626-168628276
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	ARID3A	chr2:168590304-168590631	HepG2	liver:	n/a	n/a
2	BACH1	chr2:168606202-168606504	H1-hESC	embryonic stem cell:	n/a	chr2:168606365-168606379
3	BACH1	chr2:168618942-168619019	K562	blood:	n/a	n/a
4	BHLHE40	chr2:168508086-168508467	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:168580518-168580785	A549	lung:	n/a	chr2:168580651-168580664 chr2:168580652-168580663 chr2:168580653-168580662
6	CEBPB	chr2:168558749-168559115	A549	lung:	n/a	chr2:168558953-168558966 chr2:168558953-168558964 chr2:168558955-168558966 chr2:168558955-168558964 chr2:168558955-168558964 chr2:168558953-168558966 chr2:168558955-168558964 chr2:168558955-168558964
7	CEBPB	chr2:168563312-168563736	ECC-1	luminal epithelium:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
8	CEBPB	chr2:168551372-168551587	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:168605536-168605855	A549	lung:	n/a	n/a
10	CEBPB	chr2:168548788-168549051	IMR90	lung:	n/a	chr2:168548926-168548939
11	CEBPB	chr2:168615989-168616315	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr2:168625390-168625604	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:168617930-168618150	HepG2	liver:	n/a	chr2:168618002-168618013 chr2:168618085-168618098
14	CEBPB	chr2:168558728-168559141	HepG2	liver:	n/a	chr2:168558953-168558966 chr2:168558953-168558964 chr2:168558955-168558966 chr2:168558955-168558964 chr2:168558741-168558753 chr2:168558955-168558964 chr2:168558953-168558966 chr2:168558955-168558964 chr2:168558955-168558964
15	CEBPB	chr2:168558718-168559130	IMR90	lung:	n/a	chr2:168558953-168558966 chr2:168558953-168558964 chr2:168558955-168558966 chr2:168558955-168558964 chr2:168558741-168558753 chr2:168558955-168558964 chr2:168558953-168558966 chr2:168558955-168558964 chr2:168558955-168558964
16	CEBPB	chr2:168553749-168554823	H1-hESC	embryonic stem cell:	n/a	chr2:168554662-168554673 chr2:168554440-168554453 chr2:168554440-168554453 chr2:168554442-168554451 chr2:168554440-168554451
17	CEBPB	chr2:168497976-168498270	IMR90	lung:	n/a	chr2:168498090-168498101 chr2:168498090-168498099 chr2:168498088-168498099
18	CEBPB	chr2:168548747-168549066	HepG2	liver:	n/a	chr2:168548926-168548939
19	CEBPB	chr2:168605536-168605830	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:168503865-168504125	A549	lung:	n/a	chr2:168503998-168504009 chr2:168503997-168504010 chr2:168503997-168504010
21	CEBPB	chr2:168558769-168559123	K562	blood:	n/a	chr2:168558953-168558966 chr2:168558953-168558964 chr2:168558955-168558966 chr2:168558955-168558964 chr2:168558955-168558964 chr2:168558953-168558966 chr2:168558955-168558964 chr2:168558955-168558964
22	CEBPB	chr2:168590304-168590531	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:168563341-168563663	Hela-S3	cervix:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
24	CEBPB	chr2:168543496-168543665	HepG2	liver:	n/a	chr2:168543595-168543606
25	CEBPB	chr2:168563346-168563669	H1-hESC	embryonic stem cell:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
26	CEBPB	chr2:168503829-168504152	HepG2	liver:	n/a	chr2:168503998-168504009 chr2:168503997-168504010 chr2:168503997-168504010
27	CEBPB	chr2:168580499-168580813	K562	blood:	n/a	chr2:168580651-168580664 chr2:168580652-168580663 chr2:168580653-168580662
28	CEBPB	chr2:168548862-168548990	A549	lung:	n/a	chr2:168548926-168548939
29	CEBPB	chr2:168563289-168563710	ECC-1	luminal epithelium:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
30	CEBPB	chr2:168563421-168563585	HepG2	liver:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
31	CEBPB	chr2:168580492-168580794	HepG2	liver:	n/a	chr2:168580651-168580664 chr2:168580652-168580663 chr2:168580653-168580662
32	CEBPB	chr2:168558779-168559105	H1-hESC	embryonic stem cell:	n/a	chr2:168558953-168558966 chr2:168558953-168558964 chr2:168558955-168558966 chr2:168558955-168558964 chr2:168558955-168558964 chr2:168558953-168558966 chr2:168558955-168558964 chr2:168558955-168558964
33	CEBPB	chr2:168497931-168498266	A549	lung:	n/a	chr2:168498090-168498101 chr2:168498090-168498099 chr2:168498088-168498099
34	CEBPB	chr2:168551434-168551561	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr2:168517567-168517613	HepG2	liver:	n/a	chr2:168517582-168517593 chr2:168517583-168517592
36	CEBPB	chr2:168503861-168504147	IMR90	lung:	n/a	chr2:168503998-168504009 chr2:168503997-168504010 chr2:168503997-168504010
37	CEBPB	chr2:168602588-168602776	HepG2	liver:	n/a	chr2:168602687-168602698 chr2:168602686-168602699
38	CEBPB	chr2:168558757-168559051	MCF-7	breast:	n/a	chr2:168558953-168558966 chr2:168558953-168558964 chr2:168558955-168558966 chr2:168558955-168558964 chr2:168558955-168558964 chr2:168558953-168558966 chr2:168558955-168558964 chr2:168558955-168558964
39	CEBPB	chr2:168563333-168563679	IMR90	lung:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
40	CEBPB	chr2:168616042-168616311	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:168605527-168605885	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:168563338-168563703	HepG2	liver:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
43	CEBPB	chr2:168563334-168563729	HepG2	liver:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
44	CEBPB	chr2:168503912-168504129	K562	blood:	n/a	chr2:168503998-168504009 chr2:168503997-168504010 chr2:168503997-168504010
45	CEBPB	chr2:168605540-168605841	IMR90	lung:	n/a	n/a
46	CEBPB	chr2:168563287-168563620	HepG2	liver:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
47	CEBPB	chr2:168616126-168616241	K562	blood:	n/a	n/a
48	CEBPB	chr2:168497944-168498269	HepG2	liver:	n/a	chr2:168498090-168498101 chr2:168498090-168498099 chr2:168498088-168498099
49	CHD2	chr2:168545954-168546236	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr2:168613031-168613230	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:168575200-168575250	SK-N-MC	brain:	n/a
2	chr2:168575200-168575250	SK-N-MC	brain:	n/a
3	chr2:168614674-168614724	HIPEpiC	eye:	n/a
4	chr2:168572814-168572864	AoSMC	blood vessel:	n/a
5	chr2:168525214-168525264	LNCaP	prostate:	n/a
6	chr2:168572728-168572778	RPTEC	kidney:	n/a
7	chr2:168572728-168572778	BE2_C	brain:	n/a
8	chr2:168572728-168572778	SK-N-MC	brain:	n/a
9	chr2:168614674-168614724	GM19239	blood:	n/a
10	chr2:168575200-168575250	PrEC	prostate:	n/a
11	chr2:168589499-168589549	SK-N-MC	brain:	n/a
12	chr2:168572728-168572778	HAEpiC	amniotic membrane:	n/a
13	chr2:168572563-168572613	Hepatocyte	liver:	n/a
14	chr2:168572728-168572778	SKMC	muscle:	n/a
15	chr2:168572728-168572778	Jurkat	blood:	n/a
16	chr2:168572517-168572567	HMEC	breast:	n/a
17	chr2:168570439-168570489	BJ	skin:	n/a
18	chr2:168572517-168572567	HEEpiC	esophagus:	n/a
19	chr2:168554345-168554395	HIPEpiC	eye:	n/a
20	chr2:168589499-168589549	Jurkat	blood:	n/a
21	chr2:168572517-168572567	HNPCEpiC	eye:	n/a
22	chr2:168609834-168609884	HCT-116	colon:	n/a
23	chr2:168572814-168572864	AG09309	skin:	n/a
24	chr2:168572563-168572613	Hela-S3	cervix:	n/a
25	chr2:168572814-168572864	Hepatocyte	liver:	n/a
26	chr2:168572814-168572864	HCM	heart:	n/a
27	chr2:168609834-168609884	HCM	heart:	n/a
28	chr2:168554345-168554395	SKMC	muscle:	n/a
29	chr2:168570439-168570489	HCM	heart:	n/a
30	chr2:168614674-168614724	ovcar-3	ovarian:	n/a
31	chr2:168572517-168572567	Hela-S3	cervix:	n/a
32	chr2:168609834-168609884	GM19239	blood:	n/a
33	chr2:168589499-168589549	U87	brain:	n/a
34	chr2:168570439-168570489	SK-N-SH	brain:	n/a
35	chr2:168589499-168589549	HAEpiC	amniotic membrane:	n/a
36	chr2:168575200-168575250	GM06990	blood:	n/a
37	chr2:168572728-168572778	SK-N-SH	brain:	n/a
38	chr2:168525214-168525264	HCPEpiC	choroid plexus:	n/a
39	chr2:168572563-168572613	CMK	blood:	n/a
40	chr2:168589499-168589549	HNPCEpiC	eye:	n/a
41	chr2:168572563-168572613	NHDF-neo	bronchial:	n/a
42	chr2:168572728-168572778	NT2-D1	testis:	n/a
43	chr2:168525214-168525264	NHDF-neo	bronchial:	n/a
44	chr2:168572814-168572864	T-47D	breast:	n/a
45	chr2:168525214-168525264	SK-N-SH_RA	brain:	n/a
46	chr2:168589499-168589549	RPTEC	kidney:	n/a
47	chr2:168575200-168575250	AG09319	gingival:	n/a
48	chr2:168572517-168572567	PFSK-1	brain:	n/a
49	chr2:168525214-168525264	GM12878	blood:	n/a
50	chr2:168589499-168589549	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:168511059..168513910-chr2:168515507..168517847,2	K562	blood:
2	chr2:168564278..168566007-chr2:168567964..168569747,3	K562	blood:
3	chr2:168617105..168619899-chr2:168623577..168626394,2	K562	blood:
4	chr2:168579362..168581960-chr2:168584319..168587254,2	K562	blood:
5	chr2:168574983..168577056-chr2:168583842..168586098,2	K562	blood:
6	chr2:168553081..168556581-chr2:168557540..168560778,3	MCF-7	breast:
7	chr2:168574983..168577056-chr2:168583842..168586098,2	K562	blood:
8	chr2:168534742..168537162-chr2:168545457..168548384,2	K562	blood:
9	chr2:168569700..168571629-chr2:168574567..168576209,2	K562	blood:
10	chr2:168553081..168556581-chr2:168557540..168560778,3	MCF-7	breast:
11	chr2:168572299..168574457-chr2:168576966..168579466,2	K562	blood:
12	chr2:168608803..168611110-chr2:168612210..168614300,2	K562	blood:
13	chr2:168597601..168599335-chr2:168787943..168789534,2	K562	blood:
14	chr2:168582986..168586218-chr2:168596539..168599402,3	K562	blood:
15	chr2:168534742..168537162-chr2:168545457..168548384,2	K562	blood:
16	chr2:168617105..168619899-chr2:168623577..168626394,2	K562	blood:
17	chr2:168564278..168566007-chr2:168567964..168569747,3	K562	blood:
18	chr2:168584586..168586912-chr2:168590277..168592484,2	K562	blood:
19	chr2:168608803..168611110-chr2:168612210..168614300,2	K562	blood:
20	chr2:168579362..168581960-chr2:168584319..168587254,2	K562	blood:
21	chr2:168511059..168513910-chr2:168515507..168517847,2	K562	blood:
22	chr2:168584586..168586912-chr2:168590277..168592484,2	K562	blood:
23	chr2:168569700..168571629-chr2:168574567..168576209,2	K562	blood:
24	chr2:168582986..168586218-chr2:168596539..168599402,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STK39-5	chr2:168505171-168505388	expReg_chr2_12378_-

Variant related genes	Relation type
CTAGE14P	TF binding region
RNU7-148P	TF binding region
CTAGE14P	CpG island
RNU7-148P	CpG island
ENSG00000214211	chromatin interactions

Extended variants
information (count: 4840 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:4840 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559588728	chr2:168482258-168482259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs138177829	chr2:168482277-168482278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547722474	chr2:168482364-168482365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs994428	chr2:168482428-168482429	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs2464038	chr2:168482443-168482444	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs201569730	chr2:168482453-168482454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs71031302	chr2:168482477-168482478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573611460	chr2:168482550-168482551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149563217	chr2:168482564-168482565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9711881	chr2:168482566-168482567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182151631	chr2:168482572-168482573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542515969	chr2:168482594-168482595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146048126	chr2:168482643-168482644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530944073	chr2:168482707-168482708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10188463	chr2:168482783-168482784	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs185937000	chr2:168482803-168482804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534341672	chr2:168482837-168482838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554513427	chr2:168482911-168482912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113679313	chr2:168482991-168482992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113065583	chr2:168483029-168483030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1653386	chr2:168483055-168483056	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs111735603	chr2:168483100-168483101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12463505	chr2:168483111-168483112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182673481	chr2:168483112-168483113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559390706	chr2:168483124-168483125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200905926	chr2:168483129-168483130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528359696	chr2:168483153-168483154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74898364	chr2:168483186-168483187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187265869	chr2:168483191-168483192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190714212	chr2:168483197-168483198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371417470	chr2:168483216-168483217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182667312	chr2:168483246-168483247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146371950	chr2:168483253-168483254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187668397	chr2:168483266-168483267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552383510	chr2:168483271-168483272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs193204274	chr2:168483272-168483273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs35929870	chr2:168483280-168483281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566256814	chr2:168483295-168483296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535360714	chr2:168483297-168483298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184732342	chr2:168483310-168483311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11883712	chr2:168483317-168483318	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs548095479	chr2:168483426-168483427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs368296366	chr2:168483453-168483454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187325627	chr2:168483464-168483465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs115975838	chr2:168483478-168483479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192278742	chr2:168483487-168483488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553098268	chr2:168483499-168483500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10165176	chr2:168483509-168483510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542139978	chr2:168483544-168483545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561637926	chr2:168483563-168483564	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
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
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
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	18414403	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neonatal seizures	20384724	CNVD
severe myoclonic epilepsy of infancy	18294202	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Pancreatic cancer	17952125	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168482200-168485200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr2:168490600-168507600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:168493600-168507600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr2:168502200-168504800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr2:168503000-168504400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr2:168503400-168507600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr2:168503600-168508200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr2:168503800-168504000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr2:168504000-168509000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr2:168504400-168507400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr2:168504800-168505600	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr2:168504800-168508000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr2:168505600-168508000	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr2:168507400-168510400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:168507600-168507800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:168507600-168507800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr2:168507600-168508000	Enhancers	Fetal Brain Male	brain
18	chr2:168507600-168508400	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr2:168507800-168508200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr2:168507800-168508200	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr2:168507800-168509400	Enhancers	HepG2	liver
22	chr2:168508000-168508400	Genic enhancers	HUES48 Cell Line	embryonic stem cell
23	chr2:168508000-168508400	Weak transcription	Fetal Brain Male	brain
24	chr2:168508000-168508800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr2:168508000-168509000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:168508000-168509000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr2:168508200-168508400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr2:168508200-168508600	Enhancers	H9 Cell Line	embryonic stem cell
29	chr2:168508200-168508800	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr2:168508200-168509400	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr2:168508400-168508600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr2:168508400-168508600	Enhancers	Fetal Brain Male	brain
33	chr2:168508400-168509000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr2:168508400-168519600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr2:168508400-168527200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:168508600-168508800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr2:168508600-168509000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:168508600-168509000	Enhancers	NH-A	brain
39	chr2:168508600-168520400	Weak transcription	Fetal Brain Male	brain
40	chr2:168508800-168511200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr2:168508800-168512400	Weak transcription	Brain Anterior Caudate	brain
42	chr2:168508800-168514400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr2:168509000-168509200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr2:168509000-168510000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr2:168509400-168510200	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr2:168510000-168510400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr2:168510000-168510600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr2:168510200-168511400	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr2:168510400-168512200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr2:168511400-168521400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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