Variant report

Variant	esv2753542
Chromosome Location	chr2:149004714-149268503
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1111)
CpG islands
(count:610)
Chromatin interactive
region (count:41)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1111 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:149266794-149267615	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:149009605-149009760	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:149168311-149168943	HepG2	liver:	n/a	n/a
4	ATF1	chr2:149259144-149259478	K562	blood:	n/a	n/a
5	ATF1	chr2:149245658-149245668	K562	blood:	n/a	n/a
6	ATF1	chr2:149255682-149255825	K562	blood:	n/a	n/a
7	ATF1	chr2:149017285-149017419	K562	blood:	n/a	n/a
8	BACH1	chr2:149030956-149031246	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:149017369-149017502	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:149267136-149267373	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:149017398-149017543	K562	blood:	n/a	n/a
12	BATF	chr2:149216849-149217127	GM12878	blood:	n/a	n/a
13	BATF	chr2:149251826-149252044	GM12878	blood:	n/a	n/a
14	BATF	chr2:149266999-149267403	GM12878	blood:	n/a	n/a
15	BCLAF1	chr2:149266979-149267394	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:149011302-149011613	K562	blood:	n/a	n/a
17	BHLHE40	chr2:149266777-149267353	HepG2	liver:	n/a	n/a
18	BHLHE40	chr2:149017230-149017473	K562	blood:	n/a	n/a
19	BHLHE40	chr2:149259096-149259591	K562	blood:	n/a	n/a
20	BHLHE40	chr2:149267085-149267339	K562	blood:	n/a	n/a
21	BHLHE40	chr2:149259165-149259472	HepG2	liver:	n/a	n/a
22	BRCA1	chr2:149266946-149267334	HepG2	liver:	n/a	n/a
23	BRCA1	chr2:149263078-149263081	HepG2	liver:	n/a	n/a
24	BRCA1	chr2:149266822-149267351	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr2:149011246-149011697	HCT-116	colon:	n/a	n/a
26	CBX3	chr2:149266747-149267315	K562	blood:	n/a	n/a
27	CBX3	chr2:149017230-149017609	K562	blood:	n/a	n/a
28	CBX3	chr2:149011244-149011646	K562	blood:	n/a	n/a
29	CCNT2	chr2:149266925-149267366	K562	blood:	n/a	n/a
30	CCNT2	chr2:149259186-149259452	K562	blood:	n/a	n/a
31	CEBPB	chr2:149017187-149017476	K562	blood:	n/a	n/a
32	CEBPB	chr2:149017261-149017445	K562	blood:	n/a	n/a
33	CEBPB	chr2:149038716-149038999	IMR90	lung:	n/a	chr2:149038862-149038873
34	CEBPB	chr2:149009717-149009766	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:149168464-149168895	HepG2	liver:	n/a	chr2:149168769-149168780
36	CEBPB	chr2:149266435-149267345	HepG2	liver:	n/a	chr2:149266792-149266805
37	CEBPB	chr2:149036854-149037024	HepG2	liver:	n/a	chr2:149036949-149036960
38	CEBPB	chr2:149107861-149108193	Hela-S3	cervix:	n/a	chr2:149107998-149108011 chr2:149108084-149108095 chr2:149108000-149108011 chr2:149108084-149108097 chr2:149107998-149108011 chr2:149108084-149108097 chr2:149108084-149108095 chr2:149107998-149108011 chr2:149108000-149108011
39	CEBPB	chr2:149118753-149118918	HepG2	liver:	n/a	chr2:149118869-149118880
40	CEBPB	chr2:149017156-149017589	MCF-7	breast:	n/a	n/a
41	CEBPB	chr2:149013329-149013838	K562	blood:	n/a	chr2:149013700-149013711
42	CEBPB	chr2:149013365-149013868	Hela-S3	cervix:	n/a	chr2:149013700-149013711
43	CEBPB	chr2:149266950-149267346	K562	blood:	n/a	n/a
44	CEBPB	chr2:149013272-149013893	IMR90	lung:	n/a	chr2:149013700-149013711
45	CEBPB	chr2:149036906-149037097	H1-hESC	embryonic stem cell:	n/a	chr2:149036949-149036960
46	CEBPB	chr2:149243427-149243432	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr2:149148788-149149317	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr2:149045883-149046183	IMR90	lung:	n/a	n/a
49	CEBPB	chr2:149266913-149267343	A549	lung:	n/a	n/a
50	CEBPB	chr2:149266885-149267397	MCF-7	breast:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:149063092-149063142	AG04449	skin:	fetal
2	chr2:149041060-149041110	GM12892	blood:	n/a
3	chr2:149215884-149215934	HNPCEpiC	eye:	n/a
4	chr2:149096527-149096577	NH-A	brain:	n/a
5	chr2:149216409-149216459	SK-N-MC	brain:	n/a
6	chr2:149267116-149267166	SK-N-SH_RA	brain:	n/a
7	chr2:149216409-149216459	LNCaP	prostate:	n/a
8	chr2:149259371-149259421	CMK	blood:	n/a
9	chr2:149215431-149215481	GM12892	blood:	n/a
10	chr2:149215884-149215934	HMEC	breast:	n/a
11	chr2:149215642-149215692	NT2-D1	testis:	n/a
12	chr2:149215535-149215585	SK-N-SH_RA	brain:	n/a
13	chr2:149259371-149259421	ProgFib	skin:	n/a
14	chr2:149215884-149215934	HCM	heart:	n/a
15	chr2:149063092-149063142	HRCEpiC	kidney:	n/a
16	chr2:149216409-149216459	BE2_C	brain:	n/a
17	chr2:149216409-149216459	NH-A	brain:	n/a
18	chr2:149259371-149259421	HAEpiC	amniotic membrane:	n/a
19	chr2:149215535-149215585	ProgFib	skin:	n/a
20	chr2:149215642-149215692	U87	brain:	n/a
21	chr2:149215642-149215692	SKMC	muscle:	n/a
22	chr2:149063092-149063142	RPTEC	kidney:	n/a
23	chr2:149215535-149215585	MCF10A-Er-Src	breast:	n/a
24	chr2:149041060-149041110	SK-N-SH_RA	brain:	n/a
25	chr2:149041060-149041110	ovcar-3	ovarian:	n/a
26	chr2:149215535-149215585	GM12878	blood:	n/a
27	chr2:149259371-149259421	HCF	heart:	n/a
28	chr2:149215535-149215585	HRCEpiC	kidney:	n/a
29	chr2:149215535-149215585	NHBE	bronchial:	n/a
30	chr2:149215884-149215934	HCPEpiC	choroid plexus:	n/a
31	chr2:149063092-149063142	ProgFib	skin:	n/a
32	chr2:149215642-149215692	HRPEpiC	eye:	n/a
33	chr2:149215535-149215585	SAEC	small airway:	n/a
34	chr2:149259371-149259421	HRE	kidney:	n/a
35	chr2:149215431-149215481	HepG2	liver:	n/a
36	chr2:149063092-149063142	AG04450	lung:	fetal
37	chr2:149041060-149041110	AG10803	skin:	n/a
38	chr2:149259371-149259421	LNCaP	prostate:	n/a
39	chr2:149041060-149041110	H1-hESC	embryonic stem cell:	embryo
40	chr2:149215884-149215934	GM12891	blood:	n/a
41	chr2:149267116-149267166	U87	brain:	n/a
42	chr2:149216409-149216459	HIPEpiC	eye:	n/a
43	chr2:149215642-149215692	HUVEC	blood vessel:	n/a
44	chr2:149215642-149215692	AG09319	gingival:	n/a
45	chr2:149063092-149063142	HAEpiC	amniotic membrane:	n/a
46	chr2:149215535-149215585	AG09319	gingival:	n/a
47	chr2:149041060-149041110	ECC-1	luminal epithelium:	n/a
48	chr2:149096527-149096577	GM06990	blood:	n/a
49	chr2:149063092-149063142	HPAEpiC	pulmonary alveolar:	n/a
50	chr2:149216409-149216459	HCF	heart:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:149239376..149241711-chr2:149247771..149249475,2	MCF-7	breast:
2	chr2:149257941..149260096-chr2:149261087..149264018,2	K562	blood:
3	chr2:148994771..148998300-chr2:149002088..149006299,3	K562	blood:
4	chr2:149257990..149260894-chr2:149265586..149267154,2	K562	blood:
5	chr2:148704147..148707130-chr2:149248171..149249711,2	K562	blood:
6	chr2:148747086..148748063-chr2:149266705..149267668,7	MCF-7	breast:
7	chr2:149239006..149241977-chr2:149242411..149245032,2	K562	blood:
8	chr15:28276602..28277139-chr2:149188463..149189398,2	MCF-7	breast:
9	chr2:148967081..148967666-chr2:149266757..149267493,2	MCF-7	breast:
10	chr2:149075837..149077502-chr2:149078187..149080957,2	K562	blood:
11	chr2:148925257..148925927-chr2:149266799..149267551,3	MCF-7	breast:
12	chr2:149235404..149238151-chr2:149241139..149243574,2	K562	blood:
13	chr2:148976677..148978352-chr2:149006227..149008013,2	MCF-7	breast:
14	chr2:148685824..148687356-chr2:149266124..149268743,2	K562	blood:
15	chr2:149224535..149226528-chr2:149230831..149232542,2	MCF-7	breast:
16	chr2:149130660..149131621-chr21:9826960..9827638,2	MCF-7	breast:
17	chr2:149257941..149260096-chr2:149261087..149264018,2	K562	blood:
18	chr17:56707881..56710421-chr2:149007960..149010940,2	K562	blood:
19	chr2:149075837..149077502-chr2:149078187..149080957,2	K562	blood:
20	chr2:148777185..148777981-chr2:149266660..149267608,2	MCF-7	breast:
21	chr2:149236787..149238551-chr2:149238732..149240365,2	MCF-7	breast:
22	chr17:56707733..56709409-chr2:149007940..149009460,7	MCF-7	breast:
23	chr2:149098190..149099193-chr8:103870990..103871561,3	MCF-7	breast:
24	chr2:148746863..148748075-chr2:149266691..149267630,3	K562	blood:
25	chr2:149261445..149263712-chr2:149268921..149270599,2	MCF-7	breast:
26	chr2:149262235..149263751-chr2:149373469..149375065,2	K562	blood:
27	chr2:149239376..149241711-chr2:149247771..149249475,2	MCF-7	breast:
28	chr17:56707748..56709669-chr2:149007960..149010940,5	MCF-7	breast:
29	chr2:148695019..148695866-chr2:149266727..149267624,3	K562	blood:
30	chr2:149244708..149247294-chr2:149251980..149254307,2	K562	blood:
31	chr2:148747289..148748018-chr2:149266484..149267635,9	MCF-7	breast:
32	chr2:149134166..149136482-chr2:149845391..149847794,2	MCF-7	breast:
33	chr17:56708470..56709572-chr2:149008937..149009960,15	MCF-7	breast:
34	chr2:149257990..149260894-chr2:149265586..149267154,2	K562	blood:
35	chr2:149244268..149247294-chr2:149251555..149254307,3	K562	blood:
36	chr2:149236787..149238551-chr2:149238732..149240365,2	MCF-7	breast:
37	chr2:149224578..149227474-chr2:149227523..149230314,3	MCF-7	breast:
38	chr2:149244708..149247294-chr2:149251980..149254307,2	K562	blood:
39	chr17:56708724..56710145-chr2:149008940..149009960,20	MCF-7	breast:
40	chr2:148996066..148998300-chr2:149002088..149004966,2	K562	blood:
41	chr2:149244268..149247294-chr2:149251555..149254307,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBD5-1	chr2:149099783-149099905	NONHSAT074872
2	lnc-ORC4-3	chr2:149053225-149054248	NONHSAT074880
3	lnc-MBD5-1	chr2:149099783-149099905	NONHSAT074878
4	lnc-MBD5-1	chr2:149215772-149216066	NONHSAT074871
5	lnc-MBD5-1	chr2:149215772-149215927	NONHSAT074872
6	lnc-EPC2-1	chr2:149262047-149262433	expReg_chr2_10621_+
7	lnc-MBD5-1	chr2:149099783-149099905	NONHSAT074871
8	lnc-MBD5-1	chr2:149215772-149215886	NONHSAT074878

No data

Variant related genes	Relation type
MBD5	TF binding region
ENSG00000212181	TF binding region
ENSG00000224007	TF binding region
MBD5	CpG island
ENSG00000212181	CpG island
ENSG00000224007	CpG island
ENSG00000115947	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000204406	chromatin interactions

Extended variants
information (count: 9297 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:9297 , 50 per page) page: 1 2 3 4 5 6 7 ... 186

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4972340	chr2:149004714-149004715	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564994512	chr2:149004722-149004723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546471264	chr2:149004725-149004726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148436099	chr2:149004731-149004732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563947094	chr2:149004753-149004754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181685846	chr2:149004756-149004757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549293830	chr2:149004759-149004760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561231567	chr2:149004824-149004825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77036566	chr2:149004826-149004827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184821288	chr2:149004846-149004847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546559786	chr2:149004869-149004870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142311817	chr2:149004895-149004896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571651964	chr2:149005144-149005145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374683888	chr2:149005147-149005148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539081271	chr2:149005153-149005154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4972341	chr2:149005158-149005159	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs371158570	chr2:149005211-149005212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569064311	chr2:149005212-149005213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201651985	chr2:149005228-149005229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs70992200	chr2:149005231-149005232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200765440	chr2:149005232-149005233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201719887	chr2:149005234-149005235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536437548	chr2:149005237-149005238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141672537	chr2:149005244-149005245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573146898	chr2:149005259-149005260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62182765	chr2:149005265-149005266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34171937	chr2:149005269-149005270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533774187	chr2:149005355-149005356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575075835	chr2:149005357-149005358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576752726	chr2:149005364-149005365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112393731	chr2:149005380-149005381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562420545	chr2:149005403-149005404	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs140114846	chr2:149005421-149005422	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs376064291	chr2:149005429-149005430	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs78447086	chr2:149005448-149005449	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs557331780	chr2:149005453-149005454	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs75661741	chr2:149005496-149005497	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs34629954	chr2:149005503-149005504	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs546596786	chr2:149005504-149005505	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs565329737	chr2:149005529-149005530	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs532382050	chr2:149005707-149005708	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs200285285	chr2:149005737-149005738	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs551089330	chr2:149005740-149005741	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs569219128	chr2:149005746-149005747	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs545453730	chr2:149005758-149005759	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs115540053	chr2:149005786-149005787	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs189753596	chr2:149005811-149005812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115979760	chr2:149005848-149005849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540474679	chr2:149005877-149005878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11692246	chr2:149005881-149005882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

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
Autism	20531469	CNVD
Autism	21865298	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2111 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148984400-149011800	Weak transcription	Gastric	stomach
2	chr2:148984800-149011800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr2:148985400-149011200	Weak transcription	Pancreas	Pancrea
4	chr2:148986800-149011600	Weak transcription	Brain Hippocampus Middle	brain
5	chr2:148990200-149011400	Weak transcription	Spleen	Spleen
6	chr2:148992600-149009600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr2:148994800-149016600	Weak transcription	Fetal Brain Male	brain
8	chr2:148995000-149019800	Weak transcription	Aorta	Aorta
9	chr2:148995000-149030800	Weak transcription	Left Ventricle	heart
10	chr2:148995200-149011000	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr2:148995200-149011400	Weak transcription	Placenta	Placenta
12	chr2:148995400-149010400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:148995400-149011200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr2:148995400-149011200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr2:148995400-149011400	Weak transcription	Rectal Smooth Muscle	rectum
16	chr2:148995400-149013400	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr2:148995400-149015200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr2:148995600-149008400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr2:148995800-149010800	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr2:148996400-149007400	Weak transcription	Primary T cells from cord blood	blood
21	chr2:148996400-149008800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr2:148996400-149010000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr2:148996400-149011400	Weak transcription	Adipose Nuclei	Adipose
24	chr2:148996400-149030400	Weak transcription	Colon Smooth Muscle	Colon
25	chr2:148997000-149012000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:148997400-149008600	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr2:148997400-149010400	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr2:148997400-149011000	Weak transcription	Fetal Kidney	kidney
29	chr2:148997600-149009600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr2:148997800-149011400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr2:148998600-149011000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr2:148998800-149009800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:148999400-149006600	Weak transcription	Primary hematopoietic stem cells	blood
34	chr2:148999400-149009600	Weak transcription	Ovary	ovary
35	chr2:148999400-149016400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr2:148999600-149005400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr2:149000600-149007600	Weak transcription	Primary B cells from cord blood	blood
38	chr2:149002600-149015600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr2:149002800-149012000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr2:149002800-149012000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr2:149002800-149016600	Weak transcription	NHLF	lung
42	chr2:149003000-149011200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:149003000-149011400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr2:149003200-149011200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr2:149003800-149011800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr2:149005400-149005800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr2:149005800-149008000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:149006000-149011200	Weak transcription	Fetal Muscle Trunk	muscle
49	chr2:149007000-149011400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:149007400-149008800	Strong transcription	Primary T cells from cord blood	blood

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