Variant report

Variant	nsv834572
Chromosome Location	chr2:235146304-235333842
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2921)
CpG islands
(count:1163)
Chromatin interactive
region (count:36)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2921 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:235319248-235319602	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:235330851-235331308	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:235197634-235197961	HepG2	liver:	n/a	n/a
4	ATF1	chr2:235273391-235273766	K562	blood:	n/a	n/a
5	ATF1	chr2:235287126-235287349	K562	blood:	n/a	n/a
6	ATF1	chr2:235178494-235178686	K562	blood:	n/a	n/a
7	ATF1	chr2:235282801-235283120	K562	blood:	n/a	chr2:235282942-235282956
8	ATF1	chr2:235201222-235201469	K562	blood:	n/a	n/a
9	ATF1	chr2:235288553-235288793	K562	blood:	n/a	n/a
10	ATF2	chr2:235242748-235243160	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr2:235199289-235199616	GM12878	blood:	n/a	n/a
12	ATF2	chr2:235199350-235199649	GM12878	blood:	n/a	n/a
13	ATF2	chr2:235201131-235201431	GM12878	blood:	n/a	n/a
14	ATF2	chr2:235217354-235217846	GM12878	blood:	n/a	n/a
15	ATF2	chr2:235242767-235243209	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr2:235197519-235197948	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr2:235197594-235198131	HepG2	liver:	n/a	chr2:235197634-235197643
18	ATF3	chr2:235216428-235217982	A549	lung:	n/a	chr2:235217621-235217632 chr2:235217622-235217629 chr2:235217619-235217630
19	ATF3	chr2:235160267-235161051	A549	lung:	n/a	chr2:235160786-235160800
20	ATF3	chr2:235330763-235331410	A549	lung:	n/a	n/a
21	ATF3	chr2:235166614-235167343	A549	lung:	n/a	n/a
22	ATF3	chr2:235271426-235272188	A549	lung:	n/a	n/a
23	ATF3	chr2:235271480-235272207	A549	lung:	n/a	n/a
24	ATF3	chr2:235166568-235167404	A549	lung:	n/a	n/a
25	ATF3	chr2:235216851-235217873	A549	lung:	n/a	chr2:235217621-235217632 chr2:235217622-235217629 chr2:235217619-235217630
26	ATF3	chr2:235330753-235331420	A549	lung:	n/a	n/a
27	ATF3	chr2:235197610-235197973	HepG2	liver:	n/a	chr2:235197634-235197643
28	ATF3	chr2:235277406-235277946	A549	lung:	n/a	n/a
29	BACH1	chr2:235271544-235272327	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr2:235197566-235197884	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr2:235302378-235302423	K562	blood:	n/a	n/a
32	BACH1	chr2:235213660-235214009	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr2:235278160-235278277	K562	blood:	n/a	n/a
34	BACH1	chr2:235166846-235167057	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr2:235248214-235248473	GM12878	blood:	n/a	chr2:235248321-235248332
36	BATF	chr2:235199316-235199658	GM12878	blood:	n/a	chr2:235199444-235199455
37	BATF	chr2:235201052-235201409	GM12878	blood:	n/a	chr2:235201247-235201258
38	BATF	chr2:235217414-235217721	GM12878	blood:	n/a	n/a
39	BATF	chr2:235320449-235320817	GM12878	blood:	n/a	n/a
40	BATF	chr2:235201125-235201414	GM12878	blood:	n/a	chr2:235201247-235201258
41	BATF	chr2:235248145-235248493	GM12878	blood:	n/a	chr2:235248321-235248332
42	BCL11A	chr2:235217485-235217854	GM12878	blood:	n/a	n/a
43	BCL11A	chr2:235217431-235217805	GM12878	blood:	n/a	n/a
44	BCL11A	chr2:235201137-235201386	GM12878	blood:	n/a	chr2:235201247-235201256 chr2:235201246-235201255
45	BCL11A	chr2:235199312-235199713	GM12878	blood:	n/a	chr2:235199528-235199537
46	BCL11A	chr2:235199361-235199690	GM12878	blood:	n/a	chr2:235199528-235199537
47	BCL3	chr2:235277373-235278045	A549	lung:	n/a	n/a
48	BCL3	chr2:235154234-235154955	A549	lung:	n/a	n/a
49	BCL3	chr2:235150498-235151272	A549	lung:	n/a	n/a
50	BCL3	chr2:235166648-235167630	A549	lung:	n/a	chr2:235167519-235167526

(count:1163 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:235166931-235166981	ECC-1	luminal epithelium:	n/a
2	chr2:235272562-235272612	HEEpiC	esophagus:	n/a
3	chr2:235272562-235272612	AG04450	lung:	fetal
4	chr2:235166931-235166981	NH-A	brain:	n/a
5	chr2:235166931-235166981	ECC-1	luminal epithelium:	n/a
6	chr2:235272562-235272612	HEEpiC	esophagus:	n/a
7	chr2:235272562-235272612	AG04450	lung:	fetal
8	chr2:235166931-235166981	NH-A	brain:	n/a
9	chr2:235272562-235272612	SK-N-MC	brain:	n/a
10	chr2:235332274-235332324	RPTEC	kidney:	n/a
11	chr2:235156415-235156465	ECC-1	luminal epithelium:	n/a
12	chr2:235308413-235308463	U87	brain:	n/a
13	chr2:235276581-235276631	HMEC	breast:	n/a
14	chr2:235156663-235156713	SK-N-SH_RA	brain:	n/a
15	chr2:235244520-235244570	HIPEpiC	eye:	n/a
16	chr2:235200560-235200610	Hela-S3	cervix:	n/a
17	chr2:235332274-235332324	HRPEpiC	eye:	n/a
18	chr2:235244520-235244570	PFSK-1	brain:	n/a
19	chr2:235200560-235200610	PANC-1	pancreas:	n/a
20	chr2:235166931-235166981	AG10803	skin:	n/a
21	chr2:235210313-235210363	H1-hESC	embryonic stem cell:	embryo
22	chr2:235156509-235156559	HRCEpiC	kidney:	n/a
23	chr2:235319934-235319984	NHBE	bronchial:	n/a
24	chr2:235244520-235244570	Hela-S3	cervix:	n/a
25	chr2:235330993-235331043	HNPCEpiC	eye:	n/a
26	chr2:235156509-235156559	U87	brain:	n/a
27	chr2:235156663-235156713	BJ	skin:	n/a
28	chr2:235319934-235319984	HCPEpiC	choroid plexus:	n/a
29	chr2:235210313-235210363	BE2_C	brain:	n/a
30	chr2:235272562-235272612	Caco-2	colon:	n/a
31	chr2:235156415-235156465	SK-N-SH_RA	brain:	n/a
32	chr2:235332274-235332324	HL-60	blood:	n/a
33	chr2:235156415-235156465	PANC-1	pancreas:	n/a
34	chr2:235200560-235200610	HAEpiC	amniotic membrane:	n/a
35	chr2:235272562-235272612	HRE	kidney:	n/a
36	chr2:235216719-235216769	U87	brain:	n/a
37	chr2:235216719-235216769	LNCaP	prostate:	n/a
38	chr2:235319934-235319984	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:235332274-235332324	SAEC	small airway:	n/a
40	chr2:235213874-235213924	HL-60	blood:	n/a
41	chr2:235244520-235244570	ovcar-3	ovarian:	n/a
42	chr2:235308413-235308463	T-47D	breast:	n/a
43	chr2:235178208-235178258	HNPCEpiC	eye:	n/a
44	chr2:235272562-235272612	HMEC	breast:	n/a
45	chr2:235330993-235331043	HepG2	liver:	n/a
46	chr2:235319934-235319984	H1-hESC	embryonic stem cell:	embryo
47	chr2:235210313-235210363	MCF10A-Er-Src	breast:	n/a
48	chr2:235160451-235160501	RPTEC	kidney:	n/a
49	chr2:235210313-235210363	A549	lung:	n/a
50	chr2:235330993-235331043	LNCaP	prostate:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:235259968..235261569-chr2:235263374..235265184,2	MCF-7	breast:
2	chr2:235282541..235284196-chr2:235284670..235286373,2	MCF-7	breast:
3	chr2:235197413..235198142-chr2:235409239..235409759,2	K562	blood:
4	chr12:61782102..61782969-chr2:235157951..235158503,2	MCF-7	breast:
5	chr2:235233335..235235300-chr2:235237162..235239539,2	K562	blood:
6	chr2:235044065..235044622-chr2:235157381..235158015,2	MCF-7	breast:
7	chr2:235235018..235236605-chr2:235238040..235239669,2	K562	blood:
8	chr2:235198086..235200981-chr2:235203016..235204860,2	MCF-7	breast:
9	chr2:235197507..235198142-chr2:235314505..235315353,4	MCF-7	breast:
10	chr2:235198144..235199087-chr2:235301414..235302273,2	MCF-7	breast:
11	chr2:235206539..235209460-chr2:235391484..235393644,2	K562	blood:
12	chr2:235196853..235198165-chr2:235314416..235315341,7	MCF-7	breast:
13	chr2:235189626..235191968-chr2:235200515..235202999,2	K562	blood:
14	chr2:235296551..235298527-chr2:235305106..235307520,2	MCF-7	breast:
15	chr2:235197507..235198142-chr2:235314505..235315353,4	MCF-7	breast:
16	chr2:235322912..235325153-chr2:235329052..235330888,2	MCF-7	breast:
17	chr2:235201767..235203347-chr2:235209023..235210724,2	MCF-7	breast:
18	chr2:235201767..235203347-chr2:235209023..235210724,2	MCF-7	breast:
19	chr2:235282541..235284196-chr2:235284670..235286373,2	MCF-7	breast:
20	chr2:235079344..235080200-chr2:235166670..235167350,3	MCF-7	breast:
21	chr2:235197396..235198049-chr3:12430421..12431137,2	MCF-7	breast:
22	chr2:235044378..235044948-chr2:235314513..235315261,2	MCF-7	breast:
23	chr2:235189626..235191968-chr2:235200515..235202999,2	K562	blood:
24	chr2:235323512..235326074-chr2:235403865..235405439,2	MCF-7	breast:
25	chr2:235259968..235261569-chr2:235263374..235265184,2	MCF-7	breast:
26	chr2:235322912..235325153-chr2:235329052..235330888,2	MCF-7	breast:
27	chr2:235196853..235198165-chr2:235314416..235315341,7	MCF-7	breast:
28	chr2:235043979..235044965-chr2:235166466..235167435,6	MCF-7	breast:
29	chr2:235198086..235200981-chr2:235203016..235204860,2	MCF-7	breast:
30	chr2:234885292..234886125-chr2:235166874..235167410,2	MCF-7	breast:
31	chr2:235197567..235199398-chr2:235404539..235407014,2	MCF-7	breast:
32	chr2:235198144..235199087-chr2:235301414..235302273,2	MCF-7	breast:
33	chr2:235276160..235277797-chr2:235400648..235402836,2	MCF-7	breast:
34	chr2:235197644..235198199-chr2:235453526..235454186,2	MCF-7	breast:
35	chr2:235296551..235298527-chr2:235305106..235307520,2	MCF-7	breast:
36	chr2:235044193..235044936-chr2:235166707..235167413,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPP2-6	chr2:235238127-235238482	NONHSAT077531

No data

Variant related genes	Relation type
ENSG00000237784	TF binding region
ENSG00000237784	CpG island
ENSG00000188042	chromatin interactions
ENSG00000237784	chromatin interactions

Extended variants
information (count: 7837 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:7837 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs57107144	chr2:235146307-235146308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543335862	chr2:235146308-235146309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567006626	chr2:235146323-235146324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200485625	chr2:235146324-235146325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563209050	chr2:235146337-235146338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573586984	chr2:235146412-235146413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186880492	chr2:235146439-235146440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559081374	chr2:235146440-235146441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10929018	chr2:235146451-235146452	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs551147275	chr2:235146555-235146556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571100342	chr2:235146569-235146570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191775553	chr2:235146574-235146575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539662875	chr2:235146587-235146588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567993816	chr2:235146600-235146601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140419708	chr2:235146612-235146613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536923856	chr2:235146640-235146641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11886459	chr2:235146678-235146679	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs181901902	chr2:235146684-235146685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs79916183	chr2:235146741-235146742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150371167	chr2:235146798-235146799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577433567	chr2:235146806-235146807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536881337	chr2:235146819-235146820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186309572	chr2:235146827-235146828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574895549	chr2:235146828-235146829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191056188	chr2:235146856-235146857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182172877	chr2:235146861-235146862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187658672	chr2:235146918-235146919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191324232	chr2:235146937-235146938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79706729	chr2:235146976-235146977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76702495	chr2:235147063-235147064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138053315	chr2:235147114-235147115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564938105	chr2:235147127-235147128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530604169	chr2:235147138-235147139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183204072	chr2:235147146-235147147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561463130	chr2:235147147-235147148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143593972	chr2:235147150-235147151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11885494	chr2:235147187-235147188	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs146600776	chr2:235147206-235147207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532370308	chr2:235147333-235147334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188613011	chr2:235147389-235147390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569039409	chr2:235147413-235147414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs578046615	chr2:235147547-235147548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73120891	chr2:235147582-235147583	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs375585112	chr2:235147599-235147600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567078357	chr2:235147660-235147661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536549015	chr2:235147681-235147682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs117458949	chr2:235147754-235147755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572810646	chr2:235147756-235147757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191908878	chr2:235147758-235147759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558565702	chr2:235147797-235147798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	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
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Wilms tumour	21544195	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3003 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:235145000-235148600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:235145200-235149400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr2:235145200-235156000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:235146800-235147000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:235147000-235149400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:235148600-235148800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr2:235148800-235154400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:235149200-235149800	Enhancers	NHEK	skin
9	chr2:235149200-235154200	Enhancers	NH-A	brain
10	chr2:235149400-235149600	Enhancers	HUVEC	blood vessel
11	chr2:235149400-235149800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr2:235149400-235150400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:235149400-235150800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr2:235149400-235151400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr2:235149400-235151400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:235149400-235151600	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr2:235149400-235151600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr2:235149400-235151600	Enhancers	HSMM	muscle
19	chr2:235149400-235152000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr2:235149400-235152400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr2:235149400-235154400	Enhancers	Muscle Satellite Cultured Cells	--
22	chr2:235149400-235155400	Enhancers	NHDF-Ad	bronchial
23	chr2:235149400-235171600	Enhancers	HMEC	breast
24	chr2:235149600-235149800	Enhancers	Osteobl	bone
25	chr2:235149600-235150200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr2:235149600-235150600	Enhancers	A549	lung
27	chr2:235149600-235150600	Weak transcription	HUVEC	blood vessel
28	chr2:235149600-235151400	Enhancers	HSMMtube	muscle
29	chr2:235149600-235151400	Enhancers	NHLF	lung
30	chr2:235149800-235150200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr2:235149800-235150200	Flanking Active TSS	Osteobl	bone
32	chr2:235149800-235151200	Flanking Active TSS	NHEK	skin
33	chr2:235149800-235151800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:235149800-235152200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr2:235150000-235150200	Enhancers	Fetal Kidney	kidney
36	chr2:235150200-235150600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr2:235150200-235150600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr2:235150200-235151200	Weak transcription	Fetal Kidney	kidney
39	chr2:235150200-235152400	Enhancers	Osteobl	bone
40	chr2:235150400-235150800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr2:235150600-235150800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr2:235150600-235150800	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr2:235150600-235151000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr2:235150600-235151200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:235150600-235151400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:235150600-235151400	Enhancers	Hela-S3	cervix
47	chr2:235150600-235152200	Flanking Active TSS	A549	lung
48	chr2:235150600-235152400	Enhancers	HUVEC	blood vessel
49	chr2:235150800-235154000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr2:235150800-235155400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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