Variant report

Variant	nsv873077
Chromosome Location	chr1:197615391-197698103
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:508)
CpG islands
(count:0)
Chromatin interactive
region (count:59)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:197694163-197694562	K562	blood:	n/a	n/a
2	ARID3A	chr1:197644643-197644869	K562	blood:	n/a	n/a
3	ARID3A	chr1:197694328-197694543	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:197684109-197684259	HepG2	liver:	n/a	chr1:197684219-197684235
5	ARID3A	chr1:197646598-197647338	K562	blood:	n/a	n/a
6	ATF1	chr1:197692747-197692775	K562	blood:	n/a	n/a
7	ATF1	chr1:197628585-197628753	K562	blood:	n/a	n/a
8	ATF1	chr1:197662155-197662348	K562	blood:	n/a	n/a
9	ATF1	chr1:197659216-197659501	K562	blood:	n/a	n/a
10	ATF3	chr1:197659190-197659476	K562	blood:	n/a	n/a
11	BHLHE40	chr1:197644677-197645357	K562	blood:	n/a	n/a
12	BHLHE40	chr1:197675686-197675706	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:197662092-197662375	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr1:197688042-197688145	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr1:197637535-197637557	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr1:197694170-197694549	HCT-116	colon:	n/a	n/a
17	CBX3	chr1:197657398-197657712	K562	blood:	n/a	n/a
18	CBX3	chr1:197659156-197659567	K562	blood:	n/a	n/a
19	CBX3	chr1:197657426-197657826	K562	blood:	n/a	n/a
20	CBX3	chr1:197694049-197694638	K562	blood:	n/a	n/a
21	CBX3	chr1:197694104-197694578	HCT-116	colon:	n/a	n/a
22	CBX3	chr1:197694101-197694561	K562	blood:	n/a	n/a
23	CCNT2	chr1:197628837-197629021	K562	blood:	n/a	n/a
24	CEBPB	chr1:197644648-197645208	IMR90	lung:	n/a	chr1:197644801-197644814
25	CEBPB	chr1:197636033-197636389	H1-hESC	embryonic stem cell:	n/a	chr1:197636214-197636225
26	CEBPB	chr1:197636115-197636382	MCF-7	breast:	n/a	chr1:197636214-197636225
27	CEBPB	chr1:197636118-197636325	A549	lung:	n/a	chr1:197636214-197636225
28	CEBPB	chr1:197665480-197665944	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:197653542-197653769	A549	lung:	n/a	chr1:197653625-197653636 chr1:197653625-197653638 chr1:197653626-197653637 chr1:197653625-197653638 chr1:197653625-197653638
30	CEBPB	chr1:197640274-197640571	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:197665547-197665849	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:197636004-197636363	ECC-1	luminal epithelium:	n/a	chr1:197636214-197636225
33	CEBPB	chr1:197653503-197653668	Hela-S3	cervix:	n/a	chr1:197653625-197653636 chr1:197653625-197653638 chr1:197653626-197653637 chr1:197653625-197653638 chr1:197653625-197653638
34	CEBPB	chr1:197644936-197645212	A549	lung:	n/a	n/a
35	CEBPB	chr1:197635996-197636379	ECC-1	luminal epithelium:	n/a	chr1:197636214-197636225
36	CEBPB	chr1:197642631-197642770	A549	lung:	n/a	n/a
37	CEBPB	chr1:197695622-197695807	A549	lung:	n/a	n/a
38	CEBPB	chr1:197665648-197665777	HepG2	liver:	n/a	n/a
39	CEBPB	chr1:197636064-197636371	IMR90	lung:	n/a	chr1:197636214-197636225
40	CEBPB	chr1:197654916-197655252	Hela-S3	cervix:	n/a	chr1:197654954-197654965
41	CEBPB	chr1:197636120-197636397	HepG2	liver:	n/a	chr1:197636214-197636225
42	CEBPB	chr1:197636048-197636384	A549	lung:	n/a	chr1:197636214-197636225
43	CEBPB	chr1:197636102-197636374	Hela-S3	cervix:	n/a	chr1:197636214-197636225
44	CEBPB	chr1:197644728-197645255	A549	lung:	n/a	chr1:197644801-197644814
45	CEBPB	chr1:197632175-197632514	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr1:197644852-197645170	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr1:197644734-197645172	A549	lung:	n/a	chr1:197644801-197644814
48	CEBPB	chr1:197664941-197665042	HepG2	liver:	n/a	chr1:197664979-197664990
49	CEBPB	chr1:197653442-197653747	HepG2	liver:	n/a	chr1:197653625-197653636 chr1:197653625-197653638 chr1:197653626-197653637 chr1:197653625-197653638 chr1:197653625-197653638
50	CEBPB	chr1:197636043-197636378	K562	blood:	n/a	chr1:197636214-197636225

No data

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:197650384..197656370-chr1:197660434..197666309,6	K562	blood:
2	chr1:197661931..197662561-chr1:197836633..197837195,2	MCF-7	breast:
3	chr1:197645784..197649649-chr1:197651122..197654150,3	K562	blood:
4	chr1:197637854..197639785-chr1:197643428..197645113,2	K562	blood:
5	chr1:197661830..197662539-chr1:197893369..197893878,3	MCF-7	breast:
6	chr1:197620433..197622127-chr1:197700140..197702120,2	K562	blood:
7	chr1:197654756..197656407-chr1:197656576..197658427,2	MCF-7	breast:
8	chr1:197686066..197687609-chr1:197715987..197718013,2	K562	blood:
9	chr1:197613381..197615580-chr1:197616479..197618755,2	K562	blood:
10	chr1:197684119..197686608-chr1:197731962..197734836,2	MCF-7	breast:
11	chr1:197661828..197662611-chr1:197837848..197838634,2	MCF-7	breast:
12	chr1:197644483..197647407-chr1:197649632..197652293,2	K562	blood:
13	chr1:197628715..197631555-chr1:197637374..197639292,2	MCF-7	breast:
14	chr1:197685201..197688463-chr1:197690125..197692928,4	K562	blood:
15	chr1:197683448..197686429-chr1:197686441..197688273,2	K562	blood:
16	chr1:197627378..197633637-chr1:197637134..197640584,7	K562	blood:
17	chr1:197673320..197676128-chr1:197685420..197687485,2	K562	blood:
18	chr1:197654756..197656407-chr1:197656576..197658427,2	MCF-7	breast:
19	chr1:197661907..197662504-chr1:197884615..197885431,2	MCF-7	breast:
20	chr1:197631236..197632754-chr1:197743996..197746221,2	K562	blood:
21	chr1:197634768..197637407-chr1:197639641..197641579,2	K562	blood:
22	chr1:197672380..197673103-chr9:88627531..88628226,2	MCF-7	breast:
23	chr1:197674181..197674740-chr12:111020839..111021339,2	MCF-7	breast:
24	chr1:197697770..197700203-chr1:197701390..197704214,2	K562	blood:
25	chr1:197692208..197693791-chr1:197705575..197708266,2	K562	blood:
26	chr1:197652165..197657690-chr1:197657725..197663370,6	K562	blood:
27	chr1:197665354..197667881-chr1:197692912..197694722,2	K562	blood:
28	chr1:197614829..197617182-chr1:197621263..197623211,2	K562	blood:
29	chr1:197614829..197617182-chr1:197621263..197623211,2	K562	blood:
30	chr1:197661807..197662710-chr1:197837857..197838661,5	MCF-7	breast:
31	chr1:197652165..197657690-chr1:197657725..197663370,6	K562	blood:
32	chr1:197644483..197647407-chr1:197649632..197652293,2	K562	blood:
33	chr1:197688429..197690737-chr1:197693121..197696010,2	MCF-7	breast:
34	chr1:197683448..197686429-chr1:197686441..197688273,2	K562	blood:
35	chr1:197669252..197673459-chr1:197743220..197745341,4	MCF-7	breast:
36	chr1:197653272..197654957-chr1:197663523..197666309,2	K562	blood:
37	chr1:197673320..197676128-chr1:197685420..197687485,2	K562	blood:
38	chr1:197688429..197690737-chr1:197693121..197696010,2	MCF-7	breast:
39	chr1:197645784..197649649-chr1:197651122..197654150,3	K562	blood:
40	chr1:197613381..197615580-chr1:197616479..197618755,2	K562	blood:
41	chr1:197606152..197607793-chr1:197638332..197640203,2	MCF-7	breast:
42	chr1:197694509..197697349-chr1:197703943..197706021,2	MCF-7	breast:
43	chr1:197690259..197692454-chr1:197742393..197744676,2	MCF-7	breast:
44	chr1:197665354..197667881-chr1:197692912..197694722,2	K562	blood:
45	chr1:197691912..197694197-chr1:197700256..197701891,2	K562	blood:
46	chr1:197686781..197688463-chr1:197690334..197692928,2	K562	blood:
47	chr1:197634768..197637407-chr1:197639641..197641579,2	K562	blood:
48	chr1:197610998..197613034-chr1:197615077..197617017,2	MCF-7	breast:
49	chr1:197623895..197625439-chr1:197644828..197646522,2	K562	blood:
50	chr1:197685201..197688463-chr1:197690125..197692928,4	K562	blood:

No data

Variant related genes	Relation type
DENND1B	TF binding region
ENSG00000207139	TF binding region
EEF1A1P32	TF binding region
ENSG00000213047	chromatin interactions
ENSG00000143355	chromatin interactions
ENSG00000203724	chromatin interactions
ENSG00000233040	chromatin interactions
ENSG00000207139	chromatin interactions
ENSG00000196850	chromatin interactions
ENSG00000235582	chromatin interactions
ENSG00000213046	chromatin interactions

Extended variants
information (count: 2552 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2552 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1747827	chr1:197615391-197615392	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571836316	chr1:197615444-197615445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187189390	chr1:197615471-197615472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528397624	chr1:197615504-197615505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73075682	chr1:197615510-197615511	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs535851577	chr1:197615512-197615513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554194317	chr1:197615519-197615520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78829484	chr1:197615533-197615534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141649730	chr1:197615585-197615586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565121992	chr1:197615605-197615606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150531560	chr1:197615627-197615628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541362093	chr1:197615640-197615641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34496840	chr1:197615669-197615670	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs190435025	chr1:197615695-197615696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527639528	chr1:197615812-197615813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34248727	chr1:197615816-197615817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183399579	chr1:197615895-197615896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561332549	chr1:197615906-197615907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531878570	chr1:197615947-197615948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78766454	chr1:197616077-197616078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532542008	chr1:197616101-197616102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540487728	chr1:197616113-197616114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188797661	chr1:197616153-197616154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548027389	chr1:197616155-197616156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547433974	chr1:197616180-197616181	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370951684	chr1:197616185-197616186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560013540	chr1:197616186-197616187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566244721	chr1:197616284-197616285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535815423	chr1:197616308-197616309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554157303	chr1:197616333-197616334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569395209	chr1:197616344-197616345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368159546	chr1:197616352-197616353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536778289	chr1:197616404-197616405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34964882	chr1:197616495-197616496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148980029	chr1:197616518-197616519	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558467472	chr1:197616565-197616566	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577006582	chr1:197616572-197616573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs16841850	chr1:197616584-197616585	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs553206292	chr1:197616595-197616596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139529780	chr1:197616664-197616665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79726039	chr1:197616717-197616718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561297560	chr1:197616722-197616723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs193045683	chr1:197616724-197616725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543977217	chr1:197616816-197616817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149697447	chr1:197616848-197616849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146714541	chr1:197616894-197616895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547692814	chr1:197616922-197616923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566326398	chr1:197616936-197616937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370239752	chr1:197616950-197616951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113300868	chr1:197616966-197616967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	20472715	CNVD
Multiple myeloma	16461302	CNVD
Leukoplakia	24403051	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:763 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:197542000-197626400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr1:197553000-197629800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr1:197593600-197628400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr1:197596600-197644800	Weak transcription	Ovary	ovary
5	chr1:197598800-197628600	Weak transcription	NHDF-Ad	bronchial
6	chr1:197599200-197628600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr1:197602800-197625000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr1:197602800-197641400	Weak transcription	Primary B cells from peripheral blood	blood
9	chr1:197603000-197620400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr1:197603000-197621200	Weak transcription	Stomach Smooth Muscle	stomach
11	chr1:197603000-197625200	Weak transcription	Thymus	Thymus
12	chr1:197603000-197627800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr1:197603000-197628600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr1:197603000-197632400	Weak transcription	Fetal Lung	lung
15	chr1:197603000-197632600	Weak transcription	Small Intestine	intestine
16	chr1:197603200-197625000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr1:197603200-197625200	Weak transcription	Left Ventricle	heart
18	chr1:197603200-197626600	Weak transcription	Fetal Stomach	stomach
19	chr1:197603200-197628400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr1:197603200-197645000	Weak transcription	Esophagus	oesophagus
21	chr1:197603400-197618000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:197603400-197624800	Weak transcription	Right Ventricle	heart
23	chr1:197603400-197643400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr1:197604000-197626400	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr1:197604000-197628200	Weak transcription	Liver	Liver
26	chr1:197604200-197635200	Weak transcription	Aorta	Aorta
27	chr1:197604600-197626400	Weak transcription	Primary T cells from cord blood	blood
28	chr1:197607800-197622800	Weak transcription	NH-A	brain
29	chr1:197608400-197628400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr1:197608600-197631400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:197609000-197628000	Weak transcription	Fetal Kidney	kidney
32	chr1:197609600-197621600	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr1:197610200-197626200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:197610200-197640000	Weak transcription	Fetal Intestine Small	intestine
35	chr1:197610600-197622400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr1:197610800-197621000	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr1:197611800-197644800	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr1:197612000-197619400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:197612000-197622600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr1:197612000-197628200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr1:197612000-197628400	Weak transcription	Adipose Nuclei	Adipose
42	chr1:197612200-197619400	Weak transcription	Dnd41	blood
43	chr1:197612200-197642200	Weak transcription	Primary B cells from cord blood	blood
44	chr1:197612400-197628600	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr1:197612400-197628600	Weak transcription	Fetal Thymus	thymus
46	chr1:197612600-197628000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:197612800-197616000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr1:197612800-197626400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr1:197612800-197644800	Weak transcription	Fetal Intestine Large	intestine
50	chr1:197612800-197645000	Weak transcription	Sigmoid Colon	Sigmoid Colon

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