Variant report

Variant	esv3523650
Chromosome Location	chr1:179328529-179335027
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:564)
CpG islands
(count:488)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:564 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:179332575-179332913	K562	blood:	n/a	n/a
2	ARID3A	chr1:179334842-179335117	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:179334879-179335197	K562	blood:	n/a	n/a
4	ATF1	chr1:179332419-179332755	K562	blood:	n/a	n/a
5	ATF1	chr1:179334806-179335283	K562	blood:	n/a	n/a
6	ATF2	chr1:179334962-179335357	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:179334685-179335334	GM12878	blood:	n/a	n/a
8	ATF2	chr1:179334783-179335263	GM12878	blood:	n/a	n/a
9	ATF3	chr1:179334903-179335312	A549	lung:	n/a	chr1:179335081-179335091
10	ATF3	chr1:179334617-179335300	A549	lung:	n/a	chr1:179335081-179335091
11	BACH1	chr1:179334828-179335357	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:179334902-179335268	K562	blood:	n/a	n/a
13	BCL3	chr1:179334455-179335348	A549	lung:	n/a	n/a
14	BCL3	chr1:179334664-179335199	A549	lung:	n/a	n/a
15	BCLAF1	chr1:179334653-179335603	GM12878	blood:	n/a	n/a
16	BCLAF1	chr1:179334600-179335298	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:179334638-179335374	K562	blood:	n/a	chr1:179334838-179334854
18	BHLHE40	chr1:179332521-179332721	K562	blood:	n/a	n/a
19	BHLHE40	chr1:179334617-179335267	GM12878	blood:	n/a	chr1:179334838-179334854
20	BRCA1	chr1:179334746-179335254	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr1:179334845-179335276	GM12878	blood:	n/a	n/a
22	CBX3	chr1:179334429-179335515	K562	blood:	n/a	n/a
23	CCNT2	chr1:179334806-179335371	K562	blood:	n/a	n/a
24	CEBPB	chr1:179334618-179335309	A549	lung:	n/a	n/a
25	CEBPB	chr1:179334650-179335324	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr1:179334605-179335250	K562	blood:	n/a	n/a
27	CEBPB	chr1:179334632-179335327	K562	blood:	n/a	n/a
28	CEBPB	chr1:179329778-179330058	HepG2	liver:	n/a	chr1:179329888-179329901
29	CEBPB	chr1:179334708-179335283	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:179334614-179335247	A549	lung:	n/a	n/a
31	CEBPB	chr1:179334638-179335333	HepG2	liver:	n/a	n/a
32	CEBPB	chr1:179334646-179335366	HepG2	liver:	n/a	n/a
33	CEBPB	chr1:179334641-179335292	MCF-7	breast:	n/a	n/a
34	CEBPB	chr1:179334628-179335285	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:179334588-179335340	A549	lung:	n/a	n/a
36	CHD1	chr1:179334695-179335376	GM12878	blood:	n/a	n/a
37	CHD2	chr1:179334742-179335402	GM12878	blood:	n/a	n/a
38	CHD2	chr1:179334832-179335389	HepG2	liver:	n/a	n/a
39	CHD2	chr1:179334690-179335391	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr1:179334763-179335443	K562	blood:	n/a	n/a
41	CREB1	chr1:179334646-179335430	HepG2	liver:	n/a	n/a
42	CREB1	chr1:179334797-179335280	A549	lung:	n/a	n/a
43	CREB1	chr1:179334596-179335458	HepG2	liver:	n/a	n/a
44	CREB1	chr1:179334610-179335292	ECC-1	luminal epithelium:	n/a	n/a
45	CREB1	chr1:179334671-179335286	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr1:179334632-179335457	A549	lung:	n/a	n/a
47	CREB1	chr1:179334645-179335350	ECC-1	luminal epithelium:	n/a	n/a
48	CREB1	chr1:179334640-179335404	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr1:179334665-179335543	K562	blood:	n/a	n/a
50	CREB1	chr1:179334610-179335471	GM12878	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:179333987-179334037	GM12891	blood:	n/a
2	chr1:179332148-179332198	AG10803	skin:	n/a
3	chr1:179334176-179334226	A549	lung:	n/a
4	chr1:179334675-179334725	HCPEpiC	choroid plexus:	n/a
5	chr1:179334675-179334725	Hepatocyte	liver:	n/a
6	chr1:179334176-179334226	U87	brain:	n/a
7	chr1:179334176-179334226	GM12878	blood:	n/a
8	chr1:179334675-179334725	GM19239	blood:	n/a
9	chr1:179334176-179334226	AG09309	skin:	n/a
10	chr1:179334176-179334226	AG04450	lung:	fetal
11	chr1:179333589-179333639	NT2-D1	testis:	n/a
12	chr1:179333987-179334037	Caco-2	colon:	n/a
13	chr1:179333589-179333639	AG04449	skin:	fetal
14	chr1:179332148-179332198	SK-N-SH_RA	brain:	n/a
15	chr1:179334176-179334226	PFSK-1	brain:	n/a
16	chr1:179335022-179335072	GM12891	blood:	n/a
17	chr1:179334251-179334301	HMEC	breast:	n/a
18	chr1:179335022-179335072	HRE	kidney:	n/a
19	chr1:179332148-179332198	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:179334251-179334301	T-47D	breast:	n/a
21	chr1:179333987-179334037	BJ	skin:	n/a
22	chr1:179334251-179334301	SK-N-SH_RA	brain:	n/a
23	chr1:179334658-179334708	HEK293	kidney:	embryo
24	chr1:179334675-179334725	AG04449	skin:	fetal
25	chr1:179334658-179334708	H1-hESC	embryonic stem cell:	embryo
26	chr1:179334251-179334301	CMK	blood:	n/a
27	chr1:179335022-179335072	HAEpiC	amniotic membrane:	n/a
28	chr1:179334251-179334301	HEEpiC	esophagus:	n/a
29	chr1:179332148-179332198	MCF10A-Er-Src	breast:	n/a
30	chr1:179334251-179334301	GM12892	blood:	n/a
31	chr1:179334176-179334226	SK-N-MC	brain:	n/a
32	chr1:179332148-179332198	Hepatocyte	liver:	n/a
33	chr1:179333589-179333639	GM12891	blood:	n/a
34	chr1:179333987-179334037	HCT-116	colon:	n/a
35	chr1:179332148-179332198	Hela-S3	cervix:	n/a
36	chr1:179332148-179332198	AG04449	skin:	fetal
37	chr1:179333589-179333639	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:179334176-179334226	SKMC	muscle:	n/a
39	chr1:179334176-179334226	NH-A	brain:	n/a
40	chr1:179335022-179335072	CMK	blood:	n/a
41	chr1:179332148-179332198	HEEpiC	esophagus:	n/a
42	chr1:179334251-179334301	PFSK-1	brain:	n/a
43	chr1:179335022-179335072	PANC-1	pancreas:	n/a
44	chr1:179334658-179334708	PANC-1	pancreas:	n/a
45	chr1:179333589-179333639	NHBE	bronchial:	n/a
46	chr1:179334675-179334725	SK-N-SH_RA	brain:	n/a
47	chr1:179334176-179334226	LNCaP	prostate:	n/a
48	chr1:179334658-179334708	K562	blood:	n/a
49	chr1:179334251-179334301	PANC-1	pancreas:	n/a
50	chr1:179335022-179335072	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:179049160..179052033-chr1:179333339..179335895,3	K562	blood:
2	chr1:179048972..179052099-chr1:179331450..179336701,5	MCF-7	breast:
3	chr1:179303201..179305368-chr1:179327214..179329206,2	MCF-7	breast:
4	chr1:179334248..179334935-chr18:77439530..77440162,2	Hela-S3	cervix:
5	chr1:179049229..179051266-chr1:179328606..179330148,2	MCF-7	breast:
6	chr1:179319158..179320695-chr1:179327831..179330357,2	K562	blood:
7	chr1:179325938..179328666-chr1:179330165..179332477,2	K562	blood:
8	chr1:179049954..179052769-chr1:179333565..179337813,7	MCF-7	breast:
9	chr1:179323629..179325492-chr1:179329945..179332466,2	MCF-7	breast:
10	chr1:179334985..179335587-chr8:134308823..134309369,2	Hela-S3	cervix:
11	chr1:179332952..179336574-chr1:179337996..179342859,7	MCF-7	breast:
12	chr1:179315802..179317742-chr1:179327309..179329268,2	K562	blood:
13	chr1:179330939..179332441-chr1:179334465..179336040,2	MCF-7	breast:
14	chr1:179333390..179336673-chr1:179338029..179341473,3	MCF-7	breast:
15	chr1:179325938..179328666-chr1:179330165..179332477,2	K562	blood:
16	chr1:179198544..179200421-chr1:179334252..179336417,2	MCF-7	breast:
17	chr1:179260885..179265137-chr1:179333383..179339387,7	MCF-7	breast:
18	chr1:179324764..179330437-chr1:179332106..179336685,6	K562	blood:
19	chr1:179329907..179332888-chr1:179333300..179336235,2	MCF-7	breast:

No data

Variant related genes	Relation type
RN7SL374P	TF binding region
AXDND1	TF binding region
RN7SL374P	CpG island
AXDND1	CpG island
ENSG00000057252	chromatin interactions
ENSG00000104419	chromatin interactions
ENSG00000162779	chromatin interactions
ENSG00000143322	chromatin interactions
ENSG00000178412	chromatin interactions
ENSG00000263633	chromatin interactions
ENSG00000060069	chromatin interactions
ENSG00000186283	chromatin interactions

Extended variants
information (count: 255 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569901669	chr1:179328529-179328530	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs61824395	chr1:179328547-179328548	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs147302756	chr1:179328583-179328584	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs568794105	chr1:179328623-179328624	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs139214056	chr1:179328637-179328638	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs370230007	chr1:179328769-179328770	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs376581656	chr1:179328785-179328786	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs551082275	chr1:179328799-179328800	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs143318758	chr1:179328827-179328828	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs192691953	chr1:179328832-179328833	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs553338409	chr1:179328903-179328904	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs375335574	chr1:179328908-179328909	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs567045877	chr1:179328909-179328910	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs151227352	chr1:179328977-179328978	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs535806153	chr1:179328980-179328981	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs7540732	chr1:179328981-179328982	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs7529133	chr1:179329041-179329042	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs372370499	chr1:179329060-179329061	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs544585361	chr1:179329062-179329063	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs61821460	chr1:179329068-179329069	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs578109084	chr1:179329074-179329075	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs189758726	chr1:179329112-179329113	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs7529227	chr1:179329126-179329127	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs532014560	chr1:179329136-179329137	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs142059366	chr1:179329157-179329158	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs562773132	chr1:179329169-179329170	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs531221737	chr1:179329172-179329173	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs7551027	chr1:179329198-179329199	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs374859190	chr1:179329208-179329209	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs570908635	chr1:179329221-179329222	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs527425731	chr1:179329228-179329229	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs116125536	chr1:179329269-179329270	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs371601777	chr1:179329274-179329275	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs566981560	chr1:179329398-179329399	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs181303383	chr1:179329418-179329419	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs547467175	chr1:179329419-179329420	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs555804729	chr1:179329425-179329426	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs374644095	chr1:179329474-179329475	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs112344586	chr1:179329492-179329493	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs150752755	chr1:179329493-179329494	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs139085263	chr1:179329512-179329513	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs144024524	chr1:179329517-179329518	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs12024173	chr1:179329556-179329557	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs386637151	chr1:179329615-179329616	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs386637152	chr1:179329625-179329626	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs374958340	chr1:179329636-179329637	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs367673204	chr1:179329644-179329645	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs542771074	chr1:179329669-179329670	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs533019835	chr1:179329676-179329677	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs112067486	chr1:179329682-179329683	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	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
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	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
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:315 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179264800-179334200	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:179300400-179334600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr1:179305600-179334200	Weak transcription	Pancreas	Pancrea
4	chr1:179312600-179334400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr1:179314800-179334400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr1:179315000-179334400	Weak transcription	Brain Substantia Nigra	brain
7	chr1:179315000-179334400	Weak transcription	Left Ventricle	heart
8	chr1:179315400-179334400	Weak transcription	Fetal Kidney	kidney
9	chr1:179315600-179334400	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr1:179315800-179334200	Weak transcription	Fetal Thymus	thymus
11	chr1:179316000-179334000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:179316000-179334200	Weak transcription	Fetal Muscle Trunk	muscle
13	chr1:179316000-179334400	Weak transcription	Fetal Brain Female	brain
14	chr1:179316000-179334400	Weak transcription	Ovary	ovary
15	chr1:179316400-179332800	Weak transcription	Fetal Intestine Small	intestine
16	chr1:179317600-179334400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:179319200-179334400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr1:179319800-179334000	Weak transcription	HepG2	liver
19	chr1:179319800-179334200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr1:179320000-179334600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr1:179320800-179334000	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr1:179320800-179334200	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr1:179320800-179334400	Weak transcription	Fetal Lung	lung
24	chr1:179321000-179334200	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr1:179321200-179334400	Weak transcription	Fetal Stomach	stomach
26	chr1:179321200-179334400	Weak transcription	Lung	lung
27	chr1:179322400-179334200	Weak transcription	Primary B cells from cord blood	blood
28	chr1:179323000-179330600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr1:179323000-179333400	Weak transcription	Placenta	Placenta
30	chr1:179323000-179334200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr1:179323000-179334200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:179323000-179334200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr1:179323000-179334400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr1:179323000-179334400	Weak transcription	Primary hematopoietic stem cells	blood
35	chr1:179323000-179334400	Weak transcription	NH-A	brain
36	chr1:179323000-179334400	Weak transcription	Osteobl	bone
37	chr1:179323200-179330200	Weak transcription	Brain Anterior Caudate	brain
38	chr1:179323200-179330600	Weak transcription	HMEC	breast
39	chr1:179323200-179334200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr1:179323200-179334200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr1:179323200-179334200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:179323200-179334200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:179323200-179334200	Weak transcription	A549	lung
44	chr1:179323200-179334400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:179323200-179334400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr1:179323200-179334400	Weak transcription	Brain Cingulate Gyrus	brain
47	chr1:179323200-179334400	Weak transcription	Fetal Heart	heart
48	chr1:179323200-179334400	Weak transcription	Fetal Intestine Large	intestine
49	chr1:179323400-179334000	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr1:179323400-179334200	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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