Variant report

Variant	nsv875766
Chromosome Location	chr2:210996084-211033176
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	chr2:210996798-210997068	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:211032054-211032253	HepG2	liver:	n/a	chr2:211032099-211032115 chr2:211032098-211032114
3	BACH1	chr2:210998897-210999157	K562	blood:	n/a	n/a
4	BATF	chr2:210997031-210997305	GM12878	blood:	n/a	chr2:210997206-210997217
5	CEBPB	chr2:211006899-211007141	HepG2	liver:	n/a	chr2:211007014-211007025
6	CEBPB	chr2:211030469-211030550	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:211002230-211002430	HepG2	liver:	n/a	chr2:211002310-211002321 chr2:211002309-211002322 chr2:211002413-211002426
8	CEBPB	chr2:211016166-211016347	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr2:211006958-211007117	K562	blood:	n/a	chr2:211007014-211007025
10	CHD2	chr2:211011066-211011150	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr2:211008857-211008870	GM12878	blood:	n/a	n/a
12	CTCF	chr2:211023100-211023250	AG09319	gingival:	n/a	n/a
13	CTCF	chr2:211006240-211006261	LNCaP	prostate:	n/a	n/a
14	CUX1	chr2:211033153-211033859	K562	blood:	n/a	n/a
15	CUX1	chr2:211012862-211012895	K562	blood:	n/a	n/a
16	CUX1	chr2:211033117-211033308	GM12878	blood:	n/a	n/a
17	E2F4	chr2:211011236-211011553	MCF10A-Er-Src	breast:	n/a	n/a
18	EBF1	chr2:211027331-211027361	GM12878	blood:	n/a	n/a
19	EP300	chr2:211032003-211032312	SK-N-SH_RA	brain:	n/a	chr2:211032193-211032202 chr2:211032072-211032081
20	FAM48A	chr2:211028020-211028115	GM12878	blood:	n/a	n/a
21	FAM48A	chr2:211014802-211014852	GM12878	blood:	n/a	n/a
22	FOS	chr2:211032879-211033470	MCF10A-Er-Src	breast:	n/a	chr2:211033319-211033328
23	FOS	chr2:211032019-211032370	MCF10A-Er-Src	breast:	n/a	chr2:211032193-211032202 chr2:211032194-211032205 chr2:211032193-211032201 chr2:211032096-211032105 chr2:211032191-211032202 chr2:211032193-211032200
24	FOS	chr2:211032044-211032345	HUVEC	blood vessel:	n/a	chr2:211032193-211032202 chr2:211032194-211032205 chr2:211032193-211032201 chr2:211032096-211032105 chr2:211032191-211032202 chr2:211032193-211032200
25	FOS	chr2:211031914-211032446	MCF10A-Er-Src	breast:	n/a	chr2:211032193-211032202 chr2:211032194-211032205 chr2:211032193-211032201 chr2:211032096-211032105 chr2:211032191-211032202 chr2:211032193-211032200
26	FOS	chr2:211031790-211033316	MCF10A-Er-Src	breast:	n/a	chr2:211032193-211032202 chr2:211032194-211032205 chr2:211032193-211032201 chr2:211032096-211032105 chr2:211032191-211032202 chr2:211032193-211032200
27	FOS	chr2:211031967-211032494	MCF10A-Er-Src	breast:	n/a	chr2:211032193-211032202 chr2:211032194-211032205 chr2:211032193-211032201 chr2:211032096-211032105 chr2:211032191-211032202 chr2:211032193-211032200
28	FOSL1	chr2:211031843-211032449	HCT-116	colon:	n/a	chr2:211032193-211032202 chr2:211032194-211032205 chr2:211032193-211032201 chr2:211032096-211032105 chr2:211032193-211032200
29	FOXA1	chr2:210996630-210997061	HepG2	liver:	n/a	chr2:210996939-210996954
30	FOXA1	chr2:210996628-210997161	HepG2	liver:	n/a	chr2:210996939-210996954
31	FOXA2	chr2:210996551-210997339	HepG2	liver:	n/a	n/a
32	FOXA2	chr2:210996808-210997088	HepG2	liver:	n/a	n/a
33	GATA2	chr2:210997047-210997286	SH-SY5Y	brain:	n/a	chr2:210997145-210997153
34	GATA2	chr2:211022755-211023134	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr2:211007562-211007652	SH-SY5Y	brain:	n/a	n/a
36	IRF1	chr2:211031686-211031697	K562	blood:	n/a	n/a
37	IRF3	chr2:211012607-211012623	GM12878	blood:	n/a	n/a
38	JUN	chr2:211032105-211032305	HepG2	liver:	n/a	chr2:211032193-211032202 chr2:211032194-211032205 chr2:211032193-211032201 chr2:211032193-211032200
39	JUND	chr2:211031956-211032394	Hela-S3	cervix:	n/a	chr2:211032191-211032202 chr2:211032193-211032202 chr2:211032194-211032205 chr2:211032193-211032201 chr2:211032096-211032105 chr2:211032193-211032200
40	JUND	chr2:211032068-211032339	HepG2	liver:	n/a	chr2:211032191-211032202 chr2:211032193-211032202 chr2:211032194-211032205 chr2:211032193-211032201 chr2:211032096-211032105 chr2:211032193-211032200
41	JUND	chr2:211031828-211032437	HCT-116	colon:	n/a	chr2:211032191-211032202 chr2:211032193-211032202 chr2:211032194-211032205 chr2:211032193-211032201 chr2:211032096-211032105 chr2:211032193-211032200
42	MAFF	chr2:211026354-211026496	HepG2	liver:	n/a	chr2:211026453-211026471
43	MAFK	chr2:210996138-210996231	HepG2	liver:	n/a	chr2:210996201-210996215
44	MAFK	chr2:211026344-211026560	HepG2	liver:	n/a	chr2:211026455-211026470
45	MAFK	chr2:211026313-211026564	HepG2	liver:	n/a	chr2:211026455-211026470
46	MAFK	chr2:211013848-211013887	IMR90	lung:	n/a	n/a
47	MAFK	chr2:210996221-210996248	HepG2	liver:	n/a	n/a
48	MAX	chr2:211022953-211023154	NB4	blood:	n/a	chr2:211023084-211023094 chr2:211023018-211023028
49	MAX	chr2:211027319-211027717	NB4	blood:	n/a	n/a
50	MAZ	chr2:211030704-211030853	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:211018363-211018413	HRE	kidney:	n/a
2	chr2:211018363-211018413	Jurkat	blood:	n/a
3	chr2:211018363-211018413	HepG2	liver:	n/a
4	chr2:211018363-211018413	GM19239	blood:	n/a
5	chr2:211018363-211018413	MCF-7	breast:	n/a
6	chr2:211018363-211018413	SK-N-SH_RA	brain:	n/a
7	chr2:211018363-211018413	PANC-1	pancreas:	n/a
8	chr2:211018363-211018413	K562	blood:	n/a
9	chr2:211018363-211018413	HMEC	breast:	n/a
10	chr2:211018363-211018413	HCF	heart:	n/a
11	chr2:211018363-211018413	RPTEC	kidney:	n/a
12	chr2:211018363-211018413	Caco-2	colon:	n/a
13	chr2:211018363-211018413	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:211018363-211018413	AG09309	skin:	n/a
15	chr2:211018363-211018413	AG10803	skin:	n/a
16	chr2:211018363-211018413	CMK	blood:	n/a
17	chr2:211018363-211018413	NB4	blood:	n/a
18	chr2:211018363-211018413	BE2_C	brain:	n/a
19	chr2:211018363-211018413	NH-A	brain:	n/a
20	chr2:211018363-211018413	PFSK-1	brain:	n/a
21	chr2:211018363-211018413	HUVEC	blood vessel:	n/a
22	chr2:211018363-211018413	Hepatocyte	liver:	n/a
23	chr2:211018363-211018413	T-47D	breast:	n/a
24	chr2:211018363-211018413	AG09319	gingival:	n/a
25	chr2:211018363-211018413	NT2-D1	testis:	n/a
26	chr2:211018363-211018413	GM06990	blood:	n/a
27	chr2:211018363-211018413	Hela-S3	cervix:	n/a
28	chr2:211018363-211018413	HIPEpiC	eye:	n/a
29	chr2:211018363-211018413	HRPEpiC	eye:	n/a
30	chr2:211018363-211018413	SAEC	small airway:	n/a
31	chr2:211018363-211018413	HCT-116	colon:	n/a
32	chr2:211018363-211018413	SK-N-MC	brain:	n/a
33	chr2:211018363-211018413	H1-hESC	embryonic stem cell:	embryo
34	chr2:211018363-211018413	A549	lung:	n/a
35	chr2:211018363-211018413	HCM	heart:	n/a
36	chr2:211018363-211018413	HCPEpiC	choroid plexus:	n/a
37	chr2:211018363-211018413	LNCaP	prostate:	n/a
38	chr2:211018363-211018413	GM12878	blood:	n/a
39	chr2:211018363-211018413	AoSMC	blood vessel:	n/a
40	chr2:211018363-211018413	AG04449	skin:	fetal
41	chr2:211018363-211018413	BJ	skin:	n/a
42	chr2:211018363-211018413	ProgFib	skin:	n/a
43	chr2:211018363-211018413	U87	brain:	n/a
44	chr2:211018363-211018413	AG04450	lung:	fetal
45	chr2:211018363-211018413	HEK293	kidney:	embryo
46	chr2:211018363-211018413	NHBE	bronchial:	n/a
47	chr2:211018363-211018413	HEEpiC	esophagus:	n/a
48	chr2:211018363-211018413	NHDF-neo	bronchial:	n/a
49	chr2:211018363-211018413	HRCEpiC	kidney:	n/a
50	chr2:211018363-211018413	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr2:211014370..211017069-chr2:211034700..211036950,3	MCF-7	breast:
2	chr2:211009811..211011366-chr2:211033940..211036164,2	MCF-7	breast:
3	chr2:210993877..210996167-chr2:211031338..211033652,2	MCF-7	breast:
4	chr2:211032641..211035129-chr2:211036259..211038578,2	MCF-7	breast:
5	chr2:211010718..211013464-chr2:211035621..211037329,2	K562	blood:
6	chr2:210987015..210989991-chr2:211026945..211028586,2	K562	blood:
7	chr2:210993877..210996167-chr2:211031338..211033652,2	MCF-7	breast:
8	chr2:211024842..211031528-chr2:211032039..211037580,15	K562	blood:
9	chr2:211026613..211029072-chr2:211033782..211036187,2	MCF-7	breast:
10	chr2:211023987..211026400-chr2:211029886..211031396,2	K562	blood:
11	chr2:211010256..211012532-chr2:211031341..211034097,2	K562	blood:
12	chr2:211021199..211023398-chr2:211034356..211036456,2	MCF-7	breast:
13	chr2:210890364..210892703-chr2:211032232..211034302,2	K562	blood:
14	chr2:211023987..211026400-chr2:211029886..211031396,2	K562	blood:
15	chr2:211023655..211025185-chr2:211026061..211027741,2	MCF-7	breast:
16	chr2:211023133..211025046-chr2:211028754..211030676,2	MCF-7	breast:
17	chr2:211023655..211025185-chr2:211026061..211027741,2	MCF-7	breast:
18	chr2:211016855..211019287-chr2:211020625..211023750,3	K562	blood:
19	chr2:211016855..211018981-chr2:211020625..211023357,2	K562	blood:
20	chr2:211010256..211012532-chr2:211031341..211034097,2	K562	blood:
21	chr2:211030555..211032399-chr2:211034253..211036317,3	MCF-7	breast:
22	chr2:211023133..211025046-chr2:211028754..211030676,2	MCF-7	breast:
23	chr2:211024722..211030637-chr2:211032181..211037580,16	K562	blood:
24	chr2:210998511..211000664-chr2:211034718..211036371,2	MCF-7	breast:
25	chr2:211023865..211025855-chr2:211033950..211037432,3	MCF-7	breast:
26	chr2:210956589..210959472-chr2:211000390..211002980,2	MCF-7	breast:
27	chr2:211032101..211034393-chr2:211062710..211064748,2	K562	blood:
28	chr2:211020442..211023394-chr2:211033818..211036148,3	MCF-7	breast:
29	chr2:211031182..211034080-chr2:211034360..211037839,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACADL-1	chr2:211016129-211019335	NONHSAT076668
2	lnc-ACADL-1	chr2:211018907-211019335	NONHSAT076669

Variant related genes	Relation type
KANSL1L	TF binding region
ENSG00000231294	TF binding region
KANSL1L	CpG island
ENSG00000231294	CpG island
ENSG00000144445	chromatin interactions
ENSG00000231294	chromatin interactions
ENSG00000263530	chromatin interactions

Extended variants
information (count: 1269 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1269 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11893116	chr2:210996084-210996085	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551856708	chr2:210996118-210996119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569118388	chr2:210996147-210996148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531259816	chr2:210996244-210996245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186671751	chr2:210996291-210996292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79593434	chr2:210996339-210996340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34810191	chr2:210996383-210996384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369463070	chr2:210996393-210996394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372572672	chr2:210996418-210996419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368776256	chr2:210996433-210996434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78461633	chr2:210996446-210996447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76558853	chr2:210996447-210996448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78010852	chr2:210996449-210996450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553533214	chr2:210996463-210996464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375208667	chr2:210996464-210996465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191170824	chr2:210996476-210996477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570713764	chr2:210996482-210996483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375034595	chr2:210996525-210996526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184762257	chr2:210996572-210996573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556345263	chr2:210996577-210996578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190528837	chr2:210996583-210996584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574557995	chr2:210996622-210996623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569910387	chr2:210996623-210996624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555033361	chr2:210996672-210996673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574867686	chr2:210996673-210996674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182299588	chr2:210996697-210996698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560325854	chr2:210996719-210996720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185350611	chr2:210996781-210996782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543617488	chr2:210996790-210996791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77374644	chr2:210996806-210996807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139954684	chr2:210996831-210996832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373542653	chr2:210996851-210996852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562715246	chr2:210996901-210996902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545070270	chr2:210996914-210996915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190197912	chr2:210996924-210996925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548401089	chr2:210996961-210996962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149858433	chr2:210996987-210996988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557084939	chr2:210997014-210997015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs114150824	chr2:210997038-210997039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34216688	chr2:210997046-210997047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369263045	chr2:210997070-210997071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549293527	chr2:210997076-210997077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537435187	chr2:210997087-210997088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs113938524	chr2:210997090-210997091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145789338	chr2:210997093-210997094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs539715422	chr2:210997133-210997134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148562608	chr2:210997161-210997162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556510310	chr2:210997227-210997228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570002979	chr2:210997255-210997256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535625514	chr2:210997285-210997286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	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
Lung cancer	18438408	CNVD
Prostate cancer	18632612	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
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:759 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:210965000-211009800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:210978000-211010600	Weak transcription	Small Intestine	intestine
3	chr2:210978200-211009600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:210979200-211005000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:210981400-211009600	Weak transcription	Pancreas	Pancrea
6	chr2:210981400-211009800	Weak transcription	Gastric	stomach
7	chr2:210981600-211009600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:210982200-211001800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr2:210983600-211009600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:210989200-211010000	Weak transcription	Osteobl	bone
11	chr2:210990400-211010000	Weak transcription	Brain Cingulate Gyrus	brain
12	chr2:210990600-211018200	Weak transcription	Fetal Heart	heart
13	chr2:210991000-210997400	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr2:210991000-211009600	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr2:210991000-211010000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr2:210991000-211010400	Weak transcription	Fetal Brain Male	brain
17	chr2:210991000-211018200	Weak transcription	Colon Smooth Muscle	Colon
18	chr2:210991400-211009800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr2:210991400-211018200	Weak transcription	HSMMtube	muscle
20	chr2:210991800-210999000	Weak transcription	Fetal Muscle Leg	muscle
21	chr2:210991800-211011600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr2:210992200-211010000	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr2:210992400-211015000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr2:210992600-211009600	Weak transcription	Aorta	Aorta
25	chr2:210992600-211009600	Weak transcription	Fetal Stomach	stomach
26	chr2:210992600-211009600	Weak transcription	Stomach Smooth Muscle	stomach
27	chr2:210992800-210999200	Weak transcription	Primary B cells from cord blood	blood
28	chr2:210992800-211008600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr2:210992800-211008600	Weak transcription	Fetal Lung	lung
30	chr2:210992800-211009600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr2:210993000-210999600	Weak transcription	Fetal Brain Female	brain
32	chr2:210993000-211006000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr2:210993000-211009600	Weak transcription	Thymus	Thymus
34	chr2:210993400-210998800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr2:210993400-211001400	Weak transcription	Fetal Intestine Large	intestine
36	chr2:210993400-211009400	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr2:210993400-211009600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:210993400-211009600	Weak transcription	Adipose Nuclei	Adipose
39	chr2:210993400-211010000	Weak transcription	Brain Hippocampus Middle	brain
40	chr2:210994000-210996400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr2:210994000-211000400	Weak transcription	Fetal Kidney	kidney
42	chr2:210994000-211005200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr2:210994000-211009000	Weak transcription	Fetal Thymus	thymus
44	chr2:210994000-211009200	Weak transcription	Liver	Liver
45	chr2:210994000-211009400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr2:210994000-211009400	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr2:210994000-211009600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr2:210994000-211009600	Weak transcription	Ovary	ovary
49	chr2:210994000-211009600	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr2:210994000-211009800	Weak transcription	Brain Angular Gyrus	brain

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