Variant report

Variant	nsv1004663
Chromosome Location	chr2:149214090-149373061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1702)
CpG islands
(count:856)
Chromatin interactive
region (count:101)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1702 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:149300675-149300926	K562	blood:	n/a	n/a
2	ARID3A	chr2:149303207-149303376	K562	blood:	n/a	n/a
3	ARID3A	chr2:149362121-149362377	K562	blood:	n/a	n/a
4	ARID3A	chr2:149266794-149267615	HepG2	liver:	n/a	n/a
5	ATF1	chr2:149255682-149255825	K562	blood:	n/a	n/a
6	ATF1	chr2:149245658-149245668	K562	blood:	n/a	n/a
7	ATF1	chr2:149300674-149300961	K562	blood:	n/a	n/a
8	ATF1	chr2:149259144-149259478	K562	blood:	n/a	n/a
9	ATF1	chr2:149371552-149372729	K562	blood:	n/a	n/a
10	ATF2	chr2:149371817-149372698	GM12878	blood:	n/a	n/a
11	ATF2	chr2:149361008-149361559	GM12878	blood:	n/a	n/a
12	ATF2	chr2:149371740-149372753	GM12878	blood:	n/a	n/a
13	ATF2	chr2:149335544-149336105	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr2:149340733-149341112	GM12878	blood:	n/a	n/a
15	ATF2	chr2:149360929-149361523	GM12878	blood:	n/a	n/a
16	ATF2	chr2:149335593-149336053	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr2:149267136-149267373	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr2:149336096-149336371	GM12878	blood:	n/a	n/a
19	BATF	chr2:149371907-149372257	GM12878	blood:	n/a	n/a
20	BATF	chr2:149251826-149252044	GM12878	blood:	n/a	n/a
21	BATF	chr2:149348201-149348506	GM12878	blood:	n/a	chr2:149348381-149348392 chr2:149348493-149348501
22	BATF	chr2:149361082-149361544	GM12878	blood:	n/a	chr2:149361338-149361348
23	BATF	chr2:149266999-149267403	GM12878	blood:	n/a	n/a
24	BATF	chr2:149360899-149361617	GM12878	blood:	n/a	chr2:149361338-149361348
25	BATF	chr2:149348242-149348522	GM12878	blood:	n/a	chr2:149348381-149348392 chr2:149348493-149348501
26	BATF	chr2:149216849-149217127	GM12878	blood:	n/a	n/a
27	BCL11A	chr2:149335712-149336011	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCL11A	chr2:149335717-149336024	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr2:149361017-149361584	GM12878	blood:	n/a	n/a
30	BCL11A	chr2:149361128-149361468	GM12878	blood:	n/a	n/a
31	BCL3	chr2:149360924-149361487	GM12878	blood:	n/a	n/a
32	BCL3	chr2:149361034-149361531	GM12878	blood:	n/a	n/a
33	BCLAF1	chr2:149360939-149361555	GM12878	blood:	n/a	n/a
34	BCLAF1	chr2:149360965-149361601	GM12878	blood:	n/a	n/a
35	BCLAF1	chr2:149266979-149267394	GM12878	blood:	n/a	n/a
36	BHLHE40	chr2:149316237-149316437	HepG2	liver:	n/a	n/a
37	BHLHE40	chr2:149371937-149372590	K562	blood:	n/a	n/a
38	BHLHE40	chr2:149292421-149292571	K562	blood:	n/a	n/a
39	BHLHE40	chr2:149300051-149300930	K562	blood:	n/a	n/a
40	BHLHE40	chr2:149259165-149259472	HepG2	liver:	n/a	n/a
41	BHLHE40	chr2:149259096-149259591	K562	blood:	n/a	n/a
42	BHLHE40	chr2:149266777-149267353	HepG2	liver:	n/a	n/a
43	BHLHE40	chr2:149267085-149267339	K562	blood:	n/a	n/a
44	BHLHE40	chr2:149371891-149372514	GM12878	blood:	n/a	n/a
45	BHLHE40	chr2:149362081-149362383	K562	blood:	n/a	n/a
46	BHLHE40	chr2:149371502-149371695	K562	blood:	n/a	n/a
47	BHLHE40	chr2:149310469-149310500	HepG2	liver:	n/a	n/a
48	BRCA1	chr2:149274889-149274953	HepG2	liver:	n/a	n/a
49	BRCA1	chr2:149365234-149365434	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr2:149263078-149263081	HepG2	liver:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:149215431-149215481	NHDF-neo	bronchial:	n/a
2	chr2:149267116-149267166	NHBE	bronchial:	n/a
3	chr2:149215431-149215481	NHDF-neo	bronchial:	n/a
4	chr2:149267116-149267166	NHBE	bronchial:	n/a
5	chr2:149215431-149215481	AG04449	skin:	fetal
6	chr2:149215884-149215934	PrEC	prostate:	n/a
7	chr2:149282209-149282259	NHDF-neo	bronchial:	n/a
8	chr2:149270531-149270581	Hela-S3	cervix:	n/a
9	chr2:149259371-149259421	HNPCEpiC	eye:	n/a
10	chr2:149318373-149318423	Jurkat	blood:	n/a
11	chr2:149335327-149335377	K562	blood:	n/a
12	chr2:149215884-149215934	HRPEpiC	eye:	n/a
13	chr2:149310951-149311001	MCF10A-Er-Src	breast:	n/a
14	chr2:149312414-149312464	K562	blood:	n/a
15	chr2:149275796-149275846	MCF-7	breast:	n/a
16	chr2:149312414-149312464	Caco-2	colon:	n/a
17	chr2:149318373-149318423	HL-60	blood:	n/a
18	chr2:149267116-149267166	HCM	heart:	n/a
19	chr2:149215884-149215934	GM12891	blood:	n/a
20	chr2:149215884-149215934	NT2-D1	testis:	n/a
21	chr2:149259371-149259421	SK-N-SH	brain:	n/a
22	chr2:149275796-149275846	IMR90	lung:	fetal
23	chr2:149259371-149259421	NT2-D1	testis:	n/a
24	chr2:149312414-149312464	AoSMC	blood vessel:	n/a
25	chr2:149215642-149215692	AG10803	skin:	n/a
26	chr2:149216409-149216459	HRPEpiC	eye:	n/a
27	chr2:149270531-149270581	SK-N-SH_RA	brain:	n/a
28	chr2:149310951-149311001	SK-N-SH_RA	brain:	n/a
29	chr2:149267116-149267166	HCF	heart:	n/a
30	chr2:149215535-149215585	AoSMC	blood vessel:	n/a
31	chr2:149312414-149312464	IMR90	lung:	fetal
32	chr2:149216409-149216459	NHDF-neo	bronchial:	n/a
33	chr2:149216409-149216459	MCF10A-Er-Src	breast:	n/a
34	chr2:149312414-149312464	HepG2	liver:	n/a
35	chr2:149310951-149311001	HEEpiC	esophagus:	n/a
36	chr2:149259371-149259421	PFSK-1	brain:	n/a
37	chr2:149215884-149215934	BE2_C	brain:	n/a
38	chr2:149267116-149267166	SAEC	small airway:	n/a
39	chr2:149215884-149215934	Hepatocyte	liver:	n/a
40	chr2:149215535-149215585	RPTEC	kidney:	n/a
41	chr2:149312414-149312464	ProgFib	skin:	n/a
42	chr2:149335327-149335377	PrEC	prostate:	n/a
43	chr2:149310951-149311001	GM12892	blood:	n/a
44	chr2:149282209-149282259	H1-hESC	embryonic stem cell:	embryo
45	chr2:149310951-149311001	HRE	kidney:	n/a
46	chr2:149216409-149216459	SK-N-SH	brain:	n/a
47	chr2:149215642-149215692	MCF-7	breast:	n/a
48	chr2:149267116-149267166	PrEC	prostate:	n/a
49	chr2:149310951-149311001	HRPEpiC	eye:	n/a
50	chr2:149259371-149259421	GM19239	blood:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:149371306..149373545-chr2:149401234..149403326,2	MCF-7	breast:
2	chr2:149350219..149353129-chr2:149357189..149359346,2	K562	blood:
3	chr2:148777185..148777981-chr2:149266660..149267608,2	MCF-7	breast:
4	chr2:149244708..149247294-chr2:149251980..149254307,2	K562	blood:
5	chr2:149341455..149344319-chr2:149350713..149353592,2	K562	blood:
6	chr2:149281538..149284330-chr2:149286609..149289120,3	K562	blood:
7	chr2:149337761..149341729-chr2:149349251..149353355,5	MCF-7	breast:
8	chr2:149300100..149301867-chr2:149308613..149310548,2	MCF-7	breast:
9	chr2:149282589..149285549-chr2:149375360..149378026,2	MCF-7	breast:
10	chr2:149300619..149303078-chr2:149303918..149306388,2	K562	blood:
11	chr2:149366818..149368565-chr2:149369705..149372516,2	MCF-7	breast:
12	chr2:149351093..149352826-chr2:149354280..149355842,2	MCF-7	breast:
13	chr2:149365091..149367494-chr2:149401143..149403866,2	K562	blood:
14	chr2:148925257..148925927-chr2:149266799..149267551,3	MCF-7	breast:
15	chr2:149354442..149357102-chr2:149358398..149361183,2	K562	blood:
16	chr2:149348211..149350495-chr2:149361167..149362681,2	MCF-7	breast:
17	chr2:148685824..148687356-chr2:149266124..149268743,2	K562	blood:
18	chr2:149261445..149263712-chr2:149268921..149270599,2	MCF-7	breast:
19	chr2:149308756..149311819-chr2:149312294..149315148,3	K562	blood:
20	chr2:149291312..149293367-chr2:149296532..149298461,2	K562	blood:
21	chr2:149282393..149284860-chr2:149290355..149292370,2	K562	blood:
22	chr2:149300619..149303078-chr2:149303918..149306388,2	K562	blood:
23	chr2:149350363..149354072-chr2:149357506..149360712,4	MCF-7	breast:
24	chr2:149349422..149353491-chr2:149401534..149405104,5	MCF-7	breast:
25	chr2:149369055..149370598-chr2:149375055..149377127,2	MCF-7	breast:
26	chr2:149366818..149368565-chr2:149369705..149372516,2	MCF-7	breast:
27	chr2:149277983..149279760-chr2:149282502..149284169,2	K562	blood:
28	chr2:149351334..149352440-chr2:149364775..149365779,24	MCF-7	breast:
29	chr2:149286910..149287910-chrX:103028804..103029356,2	MCF-7	breast:
30	chr2:149341455..149346543-chr2:149350713..149356199,4	K562	blood:
31	chr2:149364908..149365762-chr2:149533757..149534566,3	MCF-7	breast:
32	chr2:149244268..149247294-chr2:149251555..149254307,3	K562	blood:
33	chr2:149257941..149260096-chr2:149261087..149264018,2	K562	blood:
34	chr2:149358350..149360776-chr2:149361876..149364323,2	K562	blood:
35	chr2:149244268..149247294-chr2:149251555..149254307,3	K562	blood:
36	chr2:148967081..148967666-chr2:149266757..149267493,2	MCF-7	breast:
37	chr2:149361235..149362920-chr2:149402264..149403866,2	K562	blood:
38	chr2:149239006..149241977-chr2:149242411..149245032,2	K562	blood:
39	chr2:149319544..149321447-chr2:149323434..149324991,2	MCF-7	breast:
40	chr2:149262235..149263751-chr2:149373469..149375065,2	K562	blood:
41	chr2:149224535..149226528-chr2:149230831..149232542,2	MCF-7	breast:
42	chr2:149364293..149368189-chr2:149401143..149403866,4	K562	blood:
43	chr2:149364050..149366946-chr2:149371710..149373906,2	MCF-7	breast:
44	chr2:149239376..149241711-chr2:149247771..149249475,2	MCF-7	breast:
45	chr2:149368855..149371718-chr2:149401753..149403322,2	MCF-7	breast:
46	chr2:149294626..149297219-chr2:149297327..149299085,2	K562	blood:
47	chr2:149354442..149357102-chr2:149358398..149361183,2	K562	blood:
48	chr2:149372080..149375657-chr2:149400986..149403632,3	K562	blood:
49	chr2:149294992..149296635-chr2:149307311..149309386,2	K562	blood:
50	chr2:149310604..149312256-chr2:149400996..149403979,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBD5-1	chr2:149215772-149215886	NONHSAT074878
2	lnc-MBD5-1	chr2:149215772-149215927	NONHSAT074872
3	lnc-EPC2-1	chr2:149262047-149262433	expReg_chr2_10621_+
4	lnc-MBD5-1	chr2:149215772-149216066	NONHSAT074871

No data

Variant related genes	Relation type
MBD5	TF binding region
ENSG00000232238	TF binding region
MBD5	CpG island
ENSG00000232238	CpG island
ENSG00000115947	chromatin interactions
ENSG00000123560	chromatin interactions
ENSG00000204406	chromatin interactions
ENSG00000135999	chromatin interactions
ENSG00000232238	chromatin interactions

Extended variants
information (count: 5258 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:5258 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536673010	chr2:149214250-149214251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554899310	chr2:149214324-149214325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138616527	chr2:149214327-149214328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111673354	chr2:149214332-149214333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368693147	chr2:149214357-149214358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142689050	chr2:149214402-149214403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78685489	chr2:149214409-149214410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572524096	chr2:149214450-149214451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555858056	chr2:149214463-149214464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546508559	chr2:149214479-149214480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564639861	chr2:149214480-149214481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375404039	chr2:149214484-149214485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73968630	chr2:149214572-149214573	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs77997464	chr2:149214620-149214621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75370679	chr2:149214634-149214635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73021560	chr2:149214671-149214672	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs34546123	chr2:149214731-149214732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202086491	chr2:149214756-149214757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547570513	chr2:149214778-149214779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146964338	chr2:149214825-149214826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562800789	chr2:149214841-149214842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532998882	chr2:149214857-149214858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146889008	chr2:149214865-149214866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545341368	chr2:149214886-149214887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141967322	chr2:149214914-149214915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76440350	chr2:149214928-149214929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150655098	chr2:149214972-149214973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184516602	chr2:149214985-149214986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566921308	chr2:149215027-149215028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374482938	chr2:149215090-149215091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534745482	chr2:149215093-149215094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4972365	chr2:149215139-149215140	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs140009524	chr2:149215142-149215143	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs187620761	chr2:149215165-149215166	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs558335583	chr2:149215235-149215236	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs576816093	chr2:149215380-149215381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192600573	chr2:149215404-149215405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548785734	chr2:149215414-149215415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562109706	chr2:149215491-149215492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184271709	chr2:149215543-149215544	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs189081624	chr2:149215572-149215573	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs559614905	chr2:149215595-149215596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149421955	chr2:149215638-149215639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551298530	chr2:149215683-149215684	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs569506346	chr2:149215688-149215689	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs113892972	chr2:149215689-149215690	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs548845410	chr2:149215698-149215699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566956206	chr2:149215701-149215702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534335878	chr2:149215702-149215703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537196974	chr2:149215708-149215709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
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
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	19904302	CNVD
Intellectual disability	19904302	CNVD
Microcephaly	19904302	CNVD
severe speech impairment	19904302	CNVD
Mental retardation	20152051	CNVD
2q23.1 microdeletion syndrome	18812405	CNVD
Mental retardation	19809484	CNVD
Autism	21981781	CNVD
Mental retardation	17847001	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2076 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:149174200-149221400	Weak transcription	Primary T cells from cord blood	blood
2	chr2:149174400-149221400	Weak transcription	Primary B cells from cord blood	blood
3	chr2:149193000-149226000	Weak transcription	Primary hematopoietic stem cells	blood
4	chr2:149193400-149221600	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr2:149194000-149216200	Weak transcription	Fetal Intestine Small	intestine
6	chr2:149194800-149216200	Weak transcription	Psoas Muscle	Psoas
7	chr2:149198600-149221600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr2:149198600-149226000	Weak transcription	HSMM	muscle
9	chr2:149208400-149219400	Weak transcription	Aorta	Aorta
10	chr2:149208800-149221400	Weak transcription	Ovary	ovary
11	chr2:149208800-149226200	Weak transcription	Fetal Brain Male	brain
12	chr2:149209600-149230200	Weak transcription	Small Intestine	intestine
13	chr2:149210800-149221800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr2:149210800-149227800	Weak transcription	HUVEC	blood vessel
15	chr2:149211600-149221400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr2:149212000-149221400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:149212200-149225600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr2:149213600-149214200	Enhancers	Placenta	Placenta
19	chr2:149214000-149227800	Weak transcription	HepG2	liver
20	chr2:149214200-149214600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:149214200-149221400	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr2:149214200-149225800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:149214200-149226000	Weak transcription	Placenta	Placenta
24	chr2:149214400-149226000	Weak transcription	Fetal Muscle Trunk	muscle
25	chr2:149214600-149228600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr2:149214800-149221400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr2:149214800-149221400	Weak transcription	Fetal Thymus	thymus
28	chr2:149214800-149225800	Weak transcription	Thymus	Thymus
29	chr2:149214800-149226400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:149214800-149226600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr2:149215000-149217000	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr2:149215000-149246800	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr2:149215400-149226000	Weak transcription	Brain Hippocampus Middle	brain
34	chr2:149215800-149226000	Weak transcription	Right Ventricle	heart
35	chr2:149216000-149216200	Weak transcription	Fetal Intestine Large	intestine
36	chr2:149216000-149216200	Weak transcription	Left Ventricle	heart
37	chr2:149216000-149217000	Enhancers	Placenta Amnion	Placenta Amnion
38	chr2:149216000-149224600	Weak transcription	Esophagus	oesophagus
39	chr2:149216200-149216400	Enhancers	Fetal Intestine Large	intestine
40	chr2:149216200-149216400	Enhancers	Left Ventricle	heart
41	chr2:149216200-149216400	Genic enhancers	Psoas Muscle	Psoas
42	chr2:149216200-149216400	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr2:149216200-149216600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr2:149216200-149216600	Enhancers	Fetal Intestine Small	intestine
45	chr2:149216200-149219400	Weak transcription	Colon Smooth Muscle	Colon
46	chr2:149216400-149216600	Enhancers	Psoas Muscle	Psoas
47	chr2:149216400-149216600	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr2:149216400-149217200	Enhancers	Rectal Smooth Muscle	rectum
49	chr2:149216400-149217600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr2:149216400-149221400	Weak transcription	Fetal Intestine Large	intestine

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