Variant report

Variant	nsv3176
Chromosome Location	chr1:158955373-158986568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1135)
CpG islands
(count:549)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1135 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:158979683-158980159	K562	blood:	n/a	n/a
2	ATF1	chr1:158985296-158985598	K562	blood:	n/a	n/a
3	ATF2	chr1:158969408-158969884	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr1:158985129-158985827	GM12878	blood:	n/a	n/a
5	ATF2	chr1:158985128-158985741	GM12878	blood:	n/a	n/a
6	ATF2	chr1:158978470-158978975	GM12878	blood:	n/a	n/a
7	ATF3	chr1:158985327-158985513	K562	blood:	n/a	n/a
8	BACH1	chr1:158969462-158969881	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr1:158966067-158966420	GM12878	blood:	n/a	n/a
10	BATF	chr1:158985273-158985601	GM12878	blood:	n/a	chr1:158985456-158985467
11	BATF	chr1:158966132-158966379	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:158978607-158978914	GM12878	blood:	n/a	chr1:158978887-158978896
13	BCL11A	chr1:158966081-158966327	GM12878	blood:	n/a	n/a
14	BCLAF1	chr1:158979429-158980065	GM12878	blood:	n/a	n/a
15	BCLAF1	chr1:158978480-158978976	GM12878	blood:	n/a	chr1:158978887-158978896
16	BCLAF1	chr1:158966155-158966402	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:158985083-158985898	GM12878	blood:	n/a	n/a
18	BCLAF1	chr1:158968542-158968880	GM12878	blood:	n/a	n/a
19	BCLAF1	chr1:158979353-158980167	GM12878	blood:	n/a	chr1:158979355-158979364
20	BCLAF1	chr1:158985227-158985842	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:158966157-158966444	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:158985101-158985707	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:158979236-158980038	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:158968486-158968864	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:158985290-158985648	K562	blood:	n/a	n/a
26	BHLHE40	chr1:158978511-158978916	GM12878	blood:	n/a	n/a
27	BRCA1	chr1:158978674-158978735	GM12878	blood:	n/a	n/a
28	BRCA1	chr1:158969378-158971208	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr1:158979337-158980558	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr1:158985214-158985605	K562	blood:	n/a	n/a
31	CBX3	chr1:158985291-158985578	K562	blood:	n/a	n/a
32	CCNT2	chr1:158970050-158970250	K562	blood:	n/a	n/a
33	CCNT2	chr1:158979674-158980235	K562	blood:	n/a	n/a
34	CEBPB	chr1:158979605-158979996	K562	blood:	n/a	n/a
35	CEBPB	chr1:158985267-158985623	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:158976289-158976561	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr1:158977646-158977828	H1-hESC	embryonic stem cell:	n/a	chr1:158977685-158977696 chr1:158977720-158977731
38	CEBPB	chr1:158969405-158969862	H1-hESC	embryonic stem cell:	n/a	chr1:158969611-158969623
39	CEBPB	chr1:158979563-158979997	K562	blood:	n/a	n/a
40	CEBPB	chr1:158977574-158977911	A549	lung:	n/a	chr1:158977685-158977696 chr1:158977720-158977731
41	CEBPB	chr1:158979270-158981129	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:158977586-158977904	IMR90	lung:	n/a	chr1:158977685-158977696 chr1:158977720-158977731
43	CEBPB	chr1:158969455-158970765	Hela-S3	cervix:	n/a	chr1:158969611-158969623
44	CEBPB	chr1:158985259-158985911	IMR90	lung:	n/a	chr1:158985893-158985905
45	CEBPB	chr1:158977552-158977885	Hela-S3	cervix:	n/a	chr1:158977685-158977696 chr1:158977720-158977731
46	CEBPB	chr1:158977584-158977889	HepG2	liver:	n/a	chr1:158977685-158977696 chr1:158977720-158977731
47	CEBPB	chr1:158979654-158979981	K562	blood:	n/a	n/a
48	CEBPB	chr1:158979315-158980401	IMR90	lung:	n/a	n/a
49	CEBPB	chr1:158977593-158977889	K562	blood:	n/a	chr1:158977685-158977696 chr1:158977720-158977731
50	CEBPD	chr1:158979566-158980012	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158979647-158979697	U87	brain:	n/a
2	chr1:158969712-158969762	SK-N-MC	brain:	n/a
3	chr1:158979841-158979891	SKMC	muscle:	n/a
4	chr1:158978504-158978554	HIPEpiC	eye:	n/a
5	chr1:158979810-158979860	HMEC	breast:	n/a
6	chr1:158979841-158979891	AG09309	skin:	n/a
7	chr1:158969712-158969762	A549	lung:	n/a
8	chr1:158979841-158979891	NT2-D1	testis:	n/a
9	chr1:158978468-158978518	HIPEpiC	eye:	n/a
10	chr1:158969712-158969762	MCF10A-Er-Src	breast:	n/a
11	chr1:158979841-158979891	HCM	heart:	n/a
12	chr1:158984321-158984371	HCPEpiC	choroid plexus:	n/a
13	chr1:158978504-158978554	AG04450	lung:	fetal
14	chr1:158979647-158979697	RPTEC	kidney:	n/a
15	chr1:158979647-158979697	SK-N-MC	brain:	n/a
16	chr1:158984321-158984371	BE2_C	brain:	n/a
17	chr1:158978504-158978554	HCPEpiC	choroid plexus:	n/a
18	chr1:158979647-158979697	ovcar-3	ovarian:	n/a
19	chr1:158978468-158978518	HAEpiC	amniotic membrane:	n/a
20	chr1:158969712-158969762	GM12891	blood:	n/a
21	chr1:158969712-158969762	AG09319	gingival:	n/a
22	chr1:158979538-158979588	HMEC	breast:	n/a
23	chr1:158978504-158978554	NB4	blood:	n/a
24	chr1:158979647-158979697	ECC-1	luminal epithelium:	n/a
25	chr1:158979647-158979697	NH-A	brain:	n/a
26	chr1:158978504-158978554	CMK	blood:	n/a
27	chr1:158984321-158984371	BJ	skin:	n/a
28	chr1:158978468-158978518	NHDF-neo	bronchial:	n/a
29	chr1:158979810-158979860	HUVEC	blood vessel:	n/a
30	chr1:158979538-158979588	H1-hESC	embryonic stem cell:	embryo
31	chr1:158979647-158979697	CMK	blood:	n/a
32	chr1:158979538-158979588	AG09309	skin:	n/a
33	chr1:158979810-158979860	GM06990	blood:	n/a
34	chr1:158979810-158979860	Hela-S3	cervix:	n/a
35	chr1:158978957-158979007	Caco-2	colon:	n/a
36	chr1:158984321-158984371	Jurkat	blood:	n/a
37	chr1:158978957-158979007	A549	lung:	n/a
38	chr1:158978504-158978554	Hela-S3	cervix:	n/a
39	chr1:158979810-158979860	AG04449	skin:	fetal
40	chr1:158984321-158984371	NT2-D1	testis:	n/a
41	chr1:158984321-158984371	HAEpiC	amniotic membrane:	n/a
42	chr1:158978504-158978554	HepG2	liver:	n/a
43	chr1:158979841-158979891	GM12891	blood:	n/a
44	chr1:158978957-158979007	MCF-7	breast:	n/a
45	chr1:158979647-158979697	HUVEC	blood vessel:	n/a
46	chr1:158979841-158979891	PFSK-1	brain:	n/a
47	chr1:158978957-158979007	AG04449	skin:	fetal
48	chr1:158979810-158979860	AG09309	skin:	n/a
49	chr1:158979647-158979697	T-47D	breast:	n/a
50	chr1:158984321-158984371	A549	lung:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:158475878..158476640-chr1:158968361..158968916,3	MCF-7	breast:
2	chr1:158970577..158973262-chr1:158975751..158977296,2	K562	blood:
3	chr1:158970353..158971192-chr3:169482441..169483092,2	Hela-S3	cervix:
4	chr1:158944012..158946277-chr1:158956964..158958723,2	K562	blood:
5	chr1:158954353..158956986-chr1:158959866..158962393,2	K562	blood:
6	chr1:158900682..158902203-chr1:158976628..158979178,2	K562	blood:
7	chr1:158640177..158642154-chr1:158966970..158969167,2	K562	blood:
8	chr1:158768206..158768907-chr1:158968540..158969106,3	MCF-7	breast:
9	chr1:158173526..158174221-chr1:158968084..158968716,3	MCF-7	breast:
10	chr1:158978448..158981430-chr1:159044743..159047016,2	K562	blood:
11	chr1:158980102..158980980-chr7:91467247..91467748,2	Hela-S3	cervix:
12	chr1:158476296..158476820-chr1:158968188..158969128,2	K562	blood:
13	chr1:158954353..158956986-chr1:158959866..158962635,3	K562	blood:
14	chr1:158763178..158764363-chr1:158967947..158968721,3	MCF-7	breast:
15	chr1:158954353..158956986-chr1:158959866..158962393,2	K562	blood:
16	chr1:158979699..158980284-chr16:31191231..31192125,2	Hela-S3	cervix:
17	chr1:158968169..158968975-chr1:159041872..159042414,2	K562	blood:
18	chr1:158954353..158956986-chr1:158959866..158962635,3	K562	blood:

No data

Variant related genes	Relation type
IFI16	TF binding region
IFI16	CpG island
ENSG00000163564	chromatin interactions
ENSG00000163565	chromatin interactions
ENSG00000176320	chromatin interactions
ENSG00000163568	chromatin interactions
ENSG00000270141	chromatin interactions
ENSG00000089280	chromatin interactions

Extended variants
information (count: 1202 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76061427	chr1:158955402-158955403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573375878	chr1:158955432-158955433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78905897	chr1:158955477-158955478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375606796	chr1:158955482-158955483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532539877	chr1:158955501-158955502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556114393	chr1:158955539-158955540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190250654	chr1:158955550-158955551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572735485	chr1:158955558-158955559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74230309	chr1:158955561-158955562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369965114	chr1:158955585-158955586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541342261	chr1:158955610-158955611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530169602	chr1:158955630-158955631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145653625	chr1:158955631-158955632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78386060	chr1:158955670-158955671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552041177	chr1:158955690-158955691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371494146	chr1:158955749-158955750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146628102	chr1:158955793-158955794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537446440	chr1:158955818-158955819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549707790	chr1:158955819-158955820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567977792	chr1:158955825-158955826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182546135	chr1:158955843-158955844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs578103776	chr1:158955847-158955848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185877812	chr1:158955930-158955931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557153170	chr1:158955945-158955946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573369249	chr1:158956027-158956028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189650578	chr1:158956042-158956043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545504729	chr1:158956066-158956067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534435239	chr1:158956076-158956077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181252072	chr1:158956118-158956119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141444764	chr1:158956120-158956121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544931570	chr1:158956207-158956208	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs531229254	chr1:158956211-158956212	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs562868274	chr1:158956235-158956236	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs74951717	chr1:158956265-158956266	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs542287911	chr1:158956282-158956283	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs561504852	chr1:158956297-158956298	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs560419633	chr1:158956312-158956313	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs145088395	chr1:158956323-158956324	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs541366368	chr1:158956340-158956341	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs185509944	chr1:158956393-158956394	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs570632780	chr1:158956398-158956399	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs1361567	chr1:158956412-158956413	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs190324214	chr1:158956417-158956418	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs531465201	chr1:158956433-158956434	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs370547565	chr1:158956495-158956496	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs549825891	chr1:158956497-158956498	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs138894910	chr1:158956532-158956533	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs550317658	chr1:158956544-158956545	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs547458883	chr1:158956545-158956546	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs570128166	chr1:158956571-158956572	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	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
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1491 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158949200-158956400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr1:158949800-158959400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr1:158950800-158965600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr1:158951200-158965600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr1:158952200-158955400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
6	chr1:158953400-158955800	Strong transcription	Primary T helper cells PMA-I stimulated	--
7	chr1:158953400-158960200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr1:158953600-158965400	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr1:158953600-158965600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr1:158953800-158960400	Weak transcription	Primary B cells from cord blood	blood
11	chr1:158954000-158960600	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr1:158954400-158968400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr1:158954600-158956200	Weak transcription	Aorta	Aorta
14	chr1:158955000-158968200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr1:158955200-158956000	Weak transcription	Primary T cells from cord blood	blood
16	chr1:158955400-158955800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr1:158955800-158957600	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr1:158955800-158963600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr1:158956000-158956600	Strong transcription	Primary T cells from cord blood	blood
20	chr1:158956200-158956600	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
21	chr1:158956200-158956800	ZNF genes & repeats	Aorta	Aorta
22	chr1:158956400-158956800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
23	chr1:158956400-158958200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:158956600-158961400	Weak transcription	Primary T cells from cord blood	blood
25	chr1:158956600-158966000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr1:158956800-158957000	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr1:158957000-158965800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr1:158957600-158961000	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr1:158958200-158960800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:158959400-158961000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr1:158960200-158960800	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr1:158960400-158961000	ZNF genes & repeats	Primary B cells from cord blood	blood
33	chr1:158960600-158963200	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr1:158960800-158965600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr1:158960800-158975400	Weak transcription	Spleen	Spleen
36	chr1:158961000-158961800	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr1:158961000-158965800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr1:158961000-158968200	Weak transcription	Primary B cells from cord blood	blood
39	chr1:158961400-158963000	Strong transcription	Primary T cells from cord blood	blood
40	chr1:158961800-158962000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
41	chr1:158961800-158962200	Enhancers	Placenta	Placenta
42	chr1:158962000-158965600	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr1:158963000-158968200	Weak transcription	Primary T cells from cord blood	blood
44	chr1:158963200-158965600	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr1:158963600-158965400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr1:158964800-158965000	ZNF genes & repeats	Fetal Kidney	kidney
47	chr1:158965000-158968200	Weak transcription	Fetal Kidney	kidney
48	chr1:158965400-158966000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr1:158965400-158968800	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr1:158965600-158965800	Enhancers	Primary T killer memory cells from peripheral blood	blood

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