Variant report

Variant	nsv518979
Chromosome Location	chr1:223468336-223488310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:54)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:54 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:223486540-223486668	K562	blood:	n/a	n/a
2	CBX3	chr1:223477263-223477550	K562	blood:	n/a	n/a
3	CTCF	chr1:223470940-223471090	GM12866	blood:	n/a	n/a
4	CUX1	chr1:223486586-223486802	K562	blood:	n/a	n/a
5	EBF1	chr1:223474663-223475482	GM12878	blood:	n/a	n/a
6	EBF1	chr1:223478294-223478632	GM12878	blood:	n/a	n/a
7	EBF1	chr1:223480814-223481113	GM12878	blood:	n/a	n/a
8	EBF1	chr1:223478279-223478691	GM12878	blood:	n/a	n/a
9	EBF1	chr1:223474190-223474282	GM12878	blood:	n/a	n/a
10	EP300	chr1:223479512-223479541	GM12878	blood:	n/a	n/a
11	FOS	chr1:223486423-223486617	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr1:223486414-223486652	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr1:223486445-223486535	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr1:223472086-223472369	HUVEC	blood vessel:	n/a	n/a
15	GATA1	chr1:223478561-223478830	PBDEFetal	blood:	n/a	n/a
16	GATA2	chr1:223479374-223479674	SH-SY5Y	brain:	n/a	chr1:223479554-223479563 chr1:223479551-223479567
17	GATA3	chr1:223477156-223477546	T-47D	breast:	n/a	n/a
18	GATA3	chr1:223479019-223479708	SH-SY5Y	brain:	n/a	chr1:223479554-223479563 chr1:223479551-223479567
19	GATA3	chr1:223477149-223477511	T-47D	breast:	n/a	n/a
20	JUND	chr1:223486376-223486597	K562	blood:	n/a	n/a
21	MAFF	chr1:223472946-223473247	HepG2	liver:	n/a	chr1:223473086-223473104
22	MAFF	chr1:223472983-223473260	K562	blood:	n/a	chr1:223473086-223473104
23	MAFK	chr1:223472922-223473269	IMR90	lung:	n/a	chr1:223473088-223473103
24	MAFK	chr1:223473001-223473242	HepG2	liver:	n/a	chr1:223473088-223473103
25	MAFK	chr1:223473070-223473153	Hela-S3	cervix:	n/a	chr1:223473088-223473103
26	MAFK	chr1:223472915-223473276	HepG2	liver:	n/a	chr1:223473088-223473103
27	MAFK	chr1:223472982-223473224	K562	blood:	n/a	chr1:223473088-223473103
28	MAX	chr1:223486481-223486723	K562	blood:	n/a	chr1:223486606-223486616
29	MAX	chr1:223481629-223481814	H1-hESC	embryonic stem cell:	n/a	n/a
30	MAX	chr1:223481596-223481854	H1-hESC	embryonic stem cell:	n/a	n/a
31	MAX	chr1:223486462-223486726	NB4	blood:	n/a	chr1:223486606-223486616
32	MXI1	chr1:223472040-223472562	IMR90	lung:	n/a	n/a
33	MXI1	chr1:223478352-223478480	GM12878	blood:	n/a	n/a
34	MYC	chr1:223486472-223486627	MCF10A-Er-Src	breast:	n/a	chr1:223486606-223486616
35	MYC	chr1:223486427-223486706	K562	blood:	n/a	chr1:223486606-223486616
36	NRF1	chr1:223484608-223484697	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr1:223473854-223473972	GM12878	blood:	n/a	n/a
38	POLR2A	chr1:223482548-223482585	GM12878	blood:	n/a	n/a
39	POLR2A	chr1:223475414-223475470	GM12878	blood:	n/a	n/a
40	RAD21	chr1:223472154-223472379	IMR90	lung:	n/a	n/a
41	RCOR1	chr1:223486536-223486548	K562	blood:	n/a	n/a
42	RCOR1	chr1:223471545-223472597	IMR90	lung:	n/a	n/a
43	RCOR1	chr1:223479106-223479113	GM12878	blood:	n/a	n/a
44	SPI1	chr1:223477253-223477459	GM12891	blood:	n/a	n/a
45	STAT3	chr1:223486421-223486621	MCF10A-Er-Src	breast:	n/a	n/a
46	STAT3	chr1:223484849-223485028	MCF10A-Er-Src	breast:	n/a	n/a
47	USF1	chr1:223486380-223486717	K562	blood:	n/a	n/a
48	USF1	chr1:223486334-223486814	K562	blood:	n/a	n/a
49	USF1	chr1:223486379-223486666	H1-hESC	embryonic stem cell:	n/a	n/a
50	USF1	chr1:223486315-223486731	HCT-116	colon:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:223472245-223472295	T-47D	breast:	n/a
2	chr1:223472245-223472295	Jurkat	blood:	n/a
3	chr1:223472245-223472295	MCF-7	breast:	n/a
4	chr1:223472245-223472295	SK-N-MC	brain:	n/a
5	chr1:223472245-223472295	HUVEC	blood vessel:	n/a
6	chr1:223472245-223472295	ECC-1	luminal epithelium:	n/a
7	chr1:223472245-223472295	HNPCEpiC	eye:	n/a
8	chr1:223472245-223472295	NH-A	brain:	n/a
9	chr1:223472245-223472295	HRPEpiC	eye:	n/a
10	chr1:223472245-223472295	CMK	blood:	n/a
11	chr1:223472245-223472295	HL-60	blood:	n/a
12	chr1:223472245-223472295	SK-N-SH_RA	brain:	n/a
13	chr1:223472245-223472295	AG04449	skin:	fetal
14	chr1:223472245-223472295	A549	lung:	n/a
15	chr1:223472245-223472295	Hela-S3	cervix:	n/a
16	chr1:223472245-223472295	PANC-1	pancreas:	n/a
17	chr1:223472245-223472295	NB4	blood:	n/a
18	chr1:223472245-223472295	LNCaP	prostate:	n/a
19	chr1:223472245-223472295	HCPEpiC	choroid plexus:	n/a
20	chr1:223472245-223472295	ProgFib	skin:	n/a
21	chr1:223472245-223472295	HIPEpiC	eye:	n/a
22	chr1:223472245-223472295	NHBE	bronchial:	n/a
23	chr1:223472245-223472295	HEK293	kidney:	embryo
24	chr1:223472245-223472295	Caco-2	colon:	n/a
25	chr1:223472245-223472295	AG09319	gingival:	n/a
26	chr1:223472245-223472295	AG04450	lung:	fetal
27	chr1:223472245-223472295	BJ	skin:	n/a
28	chr1:223472245-223472295	HMEC	breast:	n/a
29	chr1:223472245-223472295	HPAEpiC	pulmonary alveolar:	n/a
30	chr1:223472245-223472295	GM19239	blood:	n/a
31	chr1:223472245-223472295	U87	brain:	n/a
32	chr1:223472245-223472295	HRCEpiC	kidney:	n/a
33	chr1:223472245-223472295	SKMC	muscle:	n/a
34	chr1:223472245-223472295	K562	blood:	n/a
35	chr1:223472245-223472295	HRE	kidney:	n/a
36	chr1:223472245-223472295	HCM	heart:	n/a
37	chr1:223472245-223472295	GM06990	blood:	n/a
38	chr1:223472245-223472295	AG10803	skin:	n/a
39	chr1:223472245-223472295	NT2-D1	testis:	n/a
40	chr1:223472245-223472295	MCF10A-Er-Src	breast:	n/a
41	chr1:223472245-223472295	AoSMC	blood vessel:	n/a
42	chr1:223472245-223472295	IMR90	lung:	fetal
43	chr1:223472245-223472295	RPTEC	kidney:	n/a
44	chr1:223472245-223472295	HCF	heart:	n/a
45	chr1:223472245-223472295	HAEpiC	amniotic membrane:	n/a
46	chr1:223472245-223472295	GM12891	blood:	n/a
47	chr1:223472245-223472295	HepG2	liver:	n/a
48	chr1:223472245-223472295	SK-N-SH	brain:	n/a
49	chr1:223472245-223472295	H1-hESC	embryonic stem cell:	embryo
50	chr1:223472245-223472295	HEEpiC	esophagus:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:223482509..223485104-chr1:223493881..223496147,2	K562	blood:
2	chr1:223482285..223484073-chr1:223489102..223491218,2	K562	blood:
3	chr1:223471938..223473458-chr1:223497150..223499757,2	K562	blood:
4	chr1:223482285..223485128-chr1:223488818..223491218,2	K562	blood:
5	chr1:223472503..223474796-chr1:223478639..223480943,2	K562	blood:
6	chr1:223466621..223469312-chr1:223470297..223473880,3	K562	blood:
7	chr1:223466163..223468186-chr1:223469482..223472172,2	MCF-7	breast:
8	chr1:223466621..223469312-chr1:223470297..223473880,3	K562	blood:
9	chr1:223462981..223465642-chr1:223484099..223486031,2	MCF-7	breast:
10	chr1:223473310..223474999-chr1:223493022..223494928,2	MCF-7	breast:
11	chr1:223472503..223474796-chr1:223478639..223480943,2	K562	blood:

No data

Variant related genes	Relation type
SUSD4	TF binding region
SUSD4	CpG island

Extended variants
information (count: 659 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:659 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs712856	chr1:223468336-223468337	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs17539006	chr1:223468360-223468361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377230158	chr1:223468377-223468378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540218213	chr1:223468447-223468448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116504964	chr1:223468465-223468466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375466509	chr1:223468540-223468541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147528744	chr1:223468639-223468640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571785819	chr1:223468665-223468666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577778316	chr1:223468676-223468677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539083405	chr1:223468726-223468727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs17163777	chr1:223468732-223468733	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs566707220	chr1:223468739-223468740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533740867	chr1:223468756-223468757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555278252	chr1:223468823-223468824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573579650	chr1:223468827-223468828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373586027	chr1:223468895-223468896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78853989	chr1:223468907-223468908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555703172	chr1:223468926-223468927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188764900	chr1:223468930-223468931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565057396	chr1:223468966-223468967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140208095	chr1:223468980-223468981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34156084	chr1:223469014-223469015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192942089	chr1:223469128-223469129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76792420	chr1:223469181-223469182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs202240339	chr1:223469182-223469183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527924529	chr1:223469183-223469184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542836723	chr1:223469255-223469256	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149603957	chr1:223469260-223469261	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs17161993	chr1:223469313-223469314	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs372555654	chr1:223469354-223469355	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571622733	chr1:223469359-223469360	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201516479	chr1:223469392-223469393	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71733674	chr1:223469393-223469394	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs398053846	chr1:223469397-223469398	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185133840	chr1:223469419-223469420	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs17161994	chr1:223469434-223469435	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs566026646	chr1:223469443-223469444	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561836033	chr1:223469454-223469455	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548742282	chr1:223469567-223469568	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567236415	chr1:223469577-223469578	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144336715	chr1:223469616-223469617	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148781419	chr1:223469618-223469619	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs17518279	chr1:223469630-223469631	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs118043866	chr1:223469644-223469645	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114459990	chr1:223469703-223469704	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188800884	chr1:223469708-223469709	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572024092	chr1:223469712-223469713	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61838196	chr1:223469747-223469748	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs561427491	chr1:223469798-223469799	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576812255	chr1:223469809-223469810	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	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
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
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223443800-223472600	Weak transcription	Gastric	stomach
2	chr1:223459000-223474200	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr1:223460800-223473400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr1:223461200-223469600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr1:223464400-223472800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr1:223465800-223469600	Weak transcription	Esophagus	oesophagus
7	chr1:223466400-223471800	Weak transcription	Ovary	ovary
8	chr1:223466400-223480400	Weak transcription	Pancreas	Pancrea
9	chr1:223467200-223469200	Weak transcription	Primary T cells from cord blood	blood
10	chr1:223468600-223472000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr1:223469200-223472000	Strong transcription	Primary T cells from cord blood	blood
12	chr1:223469600-223470000	Strong transcription	Esophagus	oesophagus
13	chr1:223469600-223470000	Strong transcription	Pancreatic Islets	Pancreatic Islet
14	chr1:223470000-223472800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr1:223470000-223493200	Weak transcription	Esophagus	oesophagus
16	chr1:223471800-223472600	Enhancers	Placenta	Placenta
17	chr1:223471800-223472800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr1:223471800-223473200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr1:223471800-223473200	Enhancers	Ovary	ovary
20	chr1:223472000-223472600	Enhancers	Stomach Smooth Muscle	stomach
21	chr1:223472000-223474000	Weak transcription	Primary T cells from cord blood	blood
22	chr1:223472400-223473200	Enhancers	NH-A	brain
23	chr1:223472600-223476600	Weak transcription	Placenta	Placenta
24	chr1:223472800-223473000	Enhancers	Brain Cingulate Gyrus	brain
25	chr1:223472800-223473000	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr1:223472800-223474000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr1:223473000-223476000	Enhancers	Fetal Thymus	thymus
28	chr1:223473000-223476200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr1:223473000-223484400	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr1:223473200-223476200	Enhancers	Thymus	Thymus
31	chr1:223473400-223474200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr1:223473400-223476200	Enhancers	Primary T cells fromperipheralblood	blood
33	chr1:223473400-223476200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr1:223474000-223474800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr1:223474000-223474800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr1:223474000-223476000	Enhancers	Primary T cells from cord blood	blood
37	chr1:223474000-223476000	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr1:223474000-223476000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr1:223474000-223476000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr1:223474200-223476200	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr1:223474200-223476200	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr1:223474400-223475800	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr1:223474800-223475400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr1:223475400-223475600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr1:223475800-223480800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr1:223476000-223482000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr1:223476200-223480800	Weak transcription	Thymus	Thymus
48	chr1:223476200-223481200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr1:223476200-223481600	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr1:223476600-223477000	Enhancers	Placenta	Placenta

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