Variant report

Variant	nsv584666
Chromosome Location	chr2:231050715-231106621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1017)
CpG islands
(count:794)
Chromatin interactive
region (count:15)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1017 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:231084718-231085165	HepG2	liver:	n/a	n/a
2	ATF2	chr2:231084379-231085017	GM12878	blood:	n/a	n/a
3	ATF2	chr2:231090046-231091424	GM12878	blood:	n/a	n/a
4	ATF2	chr2:231067016-231068411	GM12878	blood:	n/a	n/a
5	ATF2	chr2:231087421-231087858	GM12878	blood:	n/a	n/a
6	ATF2	chr2:231090116-231091431	GM12878	blood:	n/a	n/a
7	ATF2	chr2:231070497-231070910	GM12878	blood:	n/a	n/a
8	ATF2	chr2:231099433-231099930	GM12878	blood:	n/a	n/a
9	ATF2	chr2:231091899-231092520	GM12878	blood:	n/a	n/a
10	ATF2	chr2:231067173-231068423	GM12878	blood:	n/a	n/a
11	ATF2	chr2:231099504-231099982	GM12878	blood:	n/a	n/a
12	BACH1	chr2:231094755-231095153	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr2:231067082-231068317	GM12878	blood:	n/a	n/a
14	BATF	chr2:231099538-231099979	GM12878	blood:	n/a	chr2:231099806-231099817 chr2:231099807-231099817
15	BATF	chr2:231081292-231081652	GM12878	blood:	n/a	n/a
16	BATF	chr2:231070416-231070879	GM12878	blood:	n/a	n/a
17	BATF	chr2:231090934-231091313	GM12878	blood:	n/a	n/a
18	BATF	chr2:231098813-231099141	GM12878	blood:	n/a	n/a
19	BATF	chr2:231067192-231067825	GM12878	blood:	n/a	n/a
20	BATF	chr2:231099544-231100002	GM12878	blood:	n/a	chr2:231099806-231099817 chr2:231099807-231099817
21	BATF	chr2:231090246-231090656	GM12878	blood:	n/a	n/a
22	BATF	chr2:231070477-231070805	GM12878	blood:	n/a	n/a
23	BATF	chr2:231090235-231090669	GM12878	blood:	n/a	n/a
24	BCL11A	chr2:231074148-231074456	GM12878	blood:	n/a	n/a
25	BCL11A	chr2:231067914-231068366	GM12878	blood:	n/a	n/a
26	BCL11A	chr2:231081280-231081473	GM12878	blood:	n/a	n/a
27	BCL11A	chr2:231099497-231099996	GM12878	blood:	n/a	chr2:231099806-231099815
28	BCL11A	chr2:231090889-231091382	GM12878	blood:	n/a	chr2:231091129-231091138
29	BCL11A	chr2:231074124-231074470	GM12878	blood:	n/a	n/a
30	BCL11A	chr2:231067150-231067836	GM12878	blood:	n/a	n/a
31	BCL11A	chr2:231090994-231091309	GM12878	blood:	n/a	chr2:231091129-231091138
32	BCL11A	chr2:231099606-231099961	GM12878	blood:	n/a	chr2:231099806-231099815
33	BCL11A	chr2:231067983-231068298	GM12878	blood:	n/a	n/a
34	BCL3	chr2:231099472-231099996	GM12878	blood:	n/a	chr2:231099806-231099815
35	BCL3	chr2:231067161-231067891	GM12878	blood:	n/a	n/a
36	BCLAF1	chr2:231090078-231091507	GM12878	blood:	n/a	chr2:231091129-231091138
37	BCLAF1	chr2:231066976-231068393	GM12878	blood:	n/a	n/a
38	BCLAF1	chr2:231090853-231091408	GM12878	blood:	n/a	chr2:231091129-231091138
39	BCLAF1	chr2:231067144-231068423	GM12878	blood:	n/a	n/a
40	BCLAF1	chr2:231090135-231090770	GM12878	blood:	n/a	n/a
41	BCLAF1	chr2:231099472-231100028	GM12878	blood:	n/a	chr2:231099806-231099815
42	BHLHE40	chr2:231091963-231092114	GM12878	blood:	n/a	n/a
43	BHLHE40	chr2:231084494-231084977	GM12878	blood:	n/a	n/a
44	BHLHE40	chr2:231090218-231090705	GM12878	blood:	n/a	n/a
45	BHLHE40	chr2:231069814-231070125	GM12878	blood:	n/a	n/a
46	BHLHE40	chr2:231084505-231085027	K562	blood:	n/a	n/a
47	BHLHE40	chr2:231064936-231065099	K562	blood:	n/a	n/a
48	BHLHE40	chr2:231091005-231091293	GM12878	blood:	n/a	n/a
49	BHLHE40	chr2:231095622-231095778	GM12878	blood:	n/a	n/a
50	BHLHE40	chr2:231074217-231074454	GM12878	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:231085725-231085775	NT2-D1	testis:	n/a
2	chr2:231085725-231085775	NT2-D1	testis:	n/a
3	chr2:231089641-231089691	RPTEC	kidney:	n/a
4	chr2:231089641-231089691	SAEC	small airway:	n/a
5	chr2:231090329-231090379	RPTEC	kidney:	n/a
6	chr2:231085725-231085775	ECC-1	luminal epithelium:	n/a
7	chr2:231084523-231084573	AoSMC	blood vessel:	n/a
8	chr2:231085735-231085785	Hela-S3	cervix:	n/a
9	chr2:231090329-231090379	ProgFib	skin:	n/a
10	chr2:231084965-231085015	ECC-1	luminal epithelium:	n/a
11	chr2:231090640-231090690	HCPEpiC	choroid plexus:	n/a
12	chr2:231085667-231085717	H1-hESC	embryonic stem cell:	embryo
13	chr2:231090531-231090581	AG09309	skin:	n/a
14	chr2:231084523-231084573	NB4	blood:	n/a
15	chr2:231085725-231085775	NHDF-neo	bronchial:	n/a
16	chr2:231090376-231090426	HepG2	liver:	n/a
17	chr2:231084941-231084991	LNCaP	prostate:	n/a
18	chr2:231084523-231084573	HAEpiC	amniotic membrane:	n/a
19	chr2:231090531-231090581	HAEpiC	amniotic membrane:	n/a
20	chr2:231090640-231090690	GM12878	blood:	n/a
21	chr2:231090329-231090379	AoSMC	blood vessel:	n/a
22	chr2:231086230-231086280	HPAEpiC	pulmonary alveolar:	n/a
23	chr2:231090329-231090379	NT2-D1	testis:	n/a
24	chr2:231085735-231085785	PANC-1	pancreas:	n/a
25	chr2:231084965-231085015	Jurkat	blood:	n/a
26	chr2:231086230-231086280	HEEpiC	esophagus:	n/a
27	chr2:231085667-231085717	HAEpiC	amniotic membrane:	n/a
28	chr2:231084965-231085015	Hepatocyte	liver:	n/a
29	chr2:231085725-231085775	PFSK-1	brain:	n/a
30	chr2:231090376-231090426	HRPEpiC	eye:	n/a
31	chr2:231089641-231089691	NB4	blood:	n/a
32	chr2:231085667-231085717	MCF10A-Er-Src	breast:	n/a
33	chr2:231085725-231085775	ProgFib	skin:	n/a
34	chr2:231090745-231090795	MCF-7	breast:	n/a
35	chr2:231084941-231084991	HCT-116	colon:	n/a
36	chr2:231090376-231090426	HAEpiC	amniotic membrane:	n/a
37	chr2:231090531-231090581	GM06990	blood:	n/a
38	chr2:231090640-231090690	NT2-D1	testis:	n/a
39	chr2:231084965-231085015	AG10803	skin:	n/a
40	chr2:231084941-231084991	BE2_C	brain:	n/a
41	chr2:231084523-231084573	BJ	skin:	n/a
42	chr2:231086230-231086280	ECC-1	luminal epithelium:	n/a
43	chr2:231085667-231085717	NB4	blood:	n/a
44	chr2:231089641-231089691	NHDF-neo	bronchial:	n/a
45	chr2:231084965-231085015	HAEpiC	amniotic membrane:	n/a
46	chr2:231084523-231084573	HEEpiC	esophagus:	n/a
47	chr2:231090376-231090426	ovcar-3	ovarian:	n/a
48	chr2:231085725-231085775	HCT-116	colon:	n/a
49	chr2:231090640-231090690	T-47D	breast:	n/a
50	chr2:231084965-231085015	HEK293	kidney:	embryo

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:231065336..231067742-chr2:231072287..231074738,2	K562	blood:
2	chr2:231081815..231083756-chr2:231088866..231091364,2	MCF-7	breast:
3	chr2:231078945..231080759-chr2:231083081..231084932,2	MCF-7	breast:
4	chr2:231072082..231074333-chr2:231080031..231082815,2	MCF-7	breast:
5	chr2:231087067..231089892-chr2:231091301..231094794,3	K562	blood:
6	chr2:231088013..231089892-chr2:231091301..231094041,2	K562	blood:
7	chr2:231082900..231084679-chr2:231088128..231090414,2	K562	blood:
8	chr2:231072082..231074333-chr2:231080031..231082815,2	MCF-7	breast:
9	chr2:231064805..231066676-chr2:231078094..231080853,2	MCF-7	breast:
10	chr2:231064688..231066515-chr2:231075264..231078231,2	K562	blood:
11	chr2:231065336..231067742-chr2:231072287..231074738,2	K562	blood:
12	chr2:231088013..231089892-chr2:231091301..231094041,2	K562	blood:
13	chr2:231087067..231089892-chr2:231091301..231094794,3	K562	blood:
14	chr2:231064805..231066676-chr2:231078094..231080853,2	MCF-7	breast:
15	chr2:231080762..231082857-chr2:231083207..231085642,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SP140-1	chr2:231106120-231106202	NONHSAT077272
2	lnc-SLC16A14-4	chr2:231072706-231072774	NONHSAT077269
3	lnc-SP140-1	chr2:231090476-231090618	NONHSAT077272
4	lnc-SP140-1	chr2:231078674-231078789	ENSG00000243565.1
5	lnc-SP140-1	chr2:231090470-231090618	ENSG00000243565.1
6	lnc-SP140-1	chr2:231078674-231078874	ENSG00000243565.1
7	lnc-SP140-1	chr2:231099653-231099681	ENSG00000243565.1
8	lnc-SLC16A14-4	chr2:231076185-231076262	NONHSAT077269
9	lnc-SP140-1	chr2:231101798-231102329	NONHSAT077273
10	lnc-SLC16A14-4	chr2:231067295-231067444	NONHSAT077269
11	lnc-SP140-1	chr2:231101799-231101975	NONHSAT077272
12	lnc-SP140-1	chr2:231102929-231103096	NONHSAT077272
13	lnc-SP140-1	chr2:231067826-231067995	ENSG00000243565.1
14	lnc-SP140-1	chr2:231090507-231090618	NONHSAT077273
15	lnc-SLC16A14-4	chr2:231065184-231065681	NONHSAT077269
16	lnc-SLC16A14-4	chr2:231074646-231074723	NONHSAT077269
17	lnc-SP140-1	chr2:231078369-231078484	ENSG00000243565.1
18	lnc-SP140-1	chr2:231078369-231078484	ENSG00000243565.1
19	lnc-SP140-1	chr2:231068340-231068409	ENSG00000243565.1

No data

Variant related genes	Relation type
SP110	TF binding region
SP140	TF binding region
SP110	CpG island
SP140	CpG island
ENSG00000079263	chromatin interactions
ENSG00000135899	chromatin interactions

Extended variants
information (count: 2100 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2100 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3948464	chr2:231050715-231050716	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556856317	chr2:231050721-231050722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145437270	chr2:231050726-231050727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140588937	chr2:231050727-231050728	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200721134	chr2:231050733-231050734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201494565	chr2:231050735-231050736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148076294	chr2:231050739-231050740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199507070	chr2:231050745-231050746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200659174	chr2:231050747-231050748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112154377	chr2:231050755-231050756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201972538	chr2:231050762-231050763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369778669	chr2:231050763-231050764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150627628	chr2:231050764-231050765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200704188	chr2:231050767-231050768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201353625	chr2:231050770-231050771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115361843	chr2:231050789-231050790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376997701	chr2:231050813-231050814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140086984	chr2:231050819-231050820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200910716	chr2:231050842-231050843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs41547617	chr2:231050870-231050871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs199850773	chr2:231050877-231050878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186820402	chr2:231050884-231050885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs202196897	chr2:231050900-231050901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368918729	chr2:231050909-231050910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138069785	chr2:231050960-231050961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199750914	chr2:231050983-231050984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112996221	chr2:231050984-231050985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189587799	chr2:231050988-231050989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs41545715	chr2:231051001-231051002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148118813	chr2:231051006-231051007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545695437	chr2:231051087-231051088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75570174	chr2:231051092-231051093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114035626	chr2:231051106-231051107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567777701	chr2:231051138-231051139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116347572	chr2:231051140-231051141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181167321	chr2:231051141-231051142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528149242	chr2:231051156-231051157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546306624	chr2:231051179-231051180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144967430	chr2:231051209-231051210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150596067	chr2:231051321-231051322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74697801	chr2:231051331-231051332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550443913	chr2:231051343-231051344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374077540	chr2:231051373-231051374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75031524	chr2:231051374-231051375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75687135	chr2:231051381-231051382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566557861	chr2:231051402-231051403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549943915	chr2:231051403-231051404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535083235	chr2:231051453-231051454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566220819	chr2:231051466-231051467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4973290	chr2:231051491-231051492	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:61)

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
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Chronic lymphocytic leukemia	21546498	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
Breast cancer	22522925	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1627 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231028400-231067000	Strong transcription	Primary B cells from peripheral blood	blood
2	chr2:231028600-231051200	Strong transcription	Primary T helper cells fromperipheralblood	blood
3	chr2:231028800-231051600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr2:231030800-231051000	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr2:231030800-231051000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr2:231031400-231051000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr2:231031400-231051000	Strong transcription	Fetal Thymus	thymus
8	chr2:231031400-231051600	Strong transcription	GM12878-XiMat	blood
9	chr2:231031400-231061200	Strong transcription	Primary B cells from cord blood	blood
10	chr2:231031600-231050800	Strong transcription	Fetal Muscle Leg	muscle
11	chr2:231031600-231052400	Weak transcription	Fetal Brain Male	brain
12	chr2:231033800-231050800	Strong transcription	Dnd41	blood
13	chr2:231035000-231051800	Strong transcription	Primary T cells from cord blood	blood
14	chr2:231035400-231077000	Weak transcription	HepG2	liver
15	chr2:231035600-231050800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr2:231035600-231050800	Strong transcription	Thymus	Thymus
17	chr2:231035600-231051000	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr2:231035600-231051000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr2:231035600-231051200	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr2:231035600-231051600	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr2:231035800-231062800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr2:231036200-231050800	Strong transcription	Duodenum Smooth Muscle	Duodenum
23	chr2:231036200-231051200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr2:231036400-231051200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr2:231036600-231051200	Strong transcription	Ovary	ovary
26	chr2:231036800-231051000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr2:231036800-231071800	Weak transcription	NHEK	skin
28	chr2:231036800-231073600	Weak transcription	HMEC	breast
29	chr2:231037200-231050800	Strong transcription	Spleen	Spleen
30	chr2:231037200-231051000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr2:231038000-231069600	Weak transcription	NHLF	lung
32	chr2:231039000-231050800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr2:231039000-231050800	Strong transcription	Fetal Stomach	stomach
34	chr2:231041400-231064600	Weak transcription	Osteobl	bone
35	chr2:231042800-231058400	Weak transcription	Brain Anterior Caudate	brain
36	chr2:231042800-231062600	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr2:231043000-231062800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr2:231043800-231057800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr2:231043800-231062600	Weak transcription	Colon Smooth Muscle	Colon
40	chr2:231044600-231062600	Weak transcription	Psoas Muscle	Psoas
41	chr2:231044800-231062600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr2:231044800-231062800	Weak transcription	Pancreas	Pancrea
43	chr2:231045000-231051000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr2:231045000-231057600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr2:231045200-231062800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr2:231046000-231062600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr2:231046200-231062600	Weak transcription	Brain Cingulate Gyrus	brain
48	chr2:231046200-231062800	Weak transcription	Right Ventricle	heart
49	chr2:231046200-231069800	Weak transcription	HSMM	muscle
50	chr2:231046400-231062400	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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