Variant report

Variant	nsv519114
Chromosome Location	chr1:167003539-167015184
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	ATF1	chr1:167013300-167013645	K562	blood:	n/a	n/a
2	ATF2	chr1:167013031-167013739	GM12878	blood:	n/a	chr1:167013480-167013491
3	ATF3	chr1:167013381-167013608	K562	blood:	n/a	chr1:167013479-167013490 chr1:167013480-167013491 chr1:167013482-167013489 chr1:167013480-167013493 chr1:167013478-167013493 chr1:167013482-167013492 chr1:167013478-167013489 chr1:167013482-167013490 chr1:167013480-167013491
4	ATF3	chr1:167013224-167013687	K562	blood:	n/a	chr1:167013479-167013490 chr1:167013480-167013491 chr1:167013482-167013489 chr1:167013480-167013493 chr1:167013478-167013493 chr1:167013482-167013492 chr1:167013478-167013489 chr1:167013482-167013490 chr1:167013480-167013491
5	BHLHE40	chr1:167013303-167013633	K562	blood:	n/a	n/a
6	BRCA1	chr1:167013471-167013493	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr1:167013171-167013672	K562	blood:	n/a	n/a
8	CCNT2	chr1:167013435-167013594	K562	blood:	n/a	n/a
9	CEBPB	chr1:167013460-167013524	K562	blood:	n/a	n/a
10	CHD2	chr1:167013444-167013454	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr1:167013450-167013619	K562	blood:	n/a	n/a
12	CHD2	chr1:167013498-167013641	HepG2	liver:	n/a	n/a
13	CREB1	chr1:167013172-167013699	GM12878	blood:	n/a	chr1:167013479-167013492
14	CREB1	chr1:167013330-167013593	H1-hESC	embryonic stem cell:	n/a	chr1:167013479-167013492
15	CREB1	chr1:167013323-167013585	A549	lung:	n/a	chr1:167013479-167013492
16	CREB1	chr1:167013268-167013673	K562	blood:	n/a	chr1:167013479-167013492
17	CREB1	chr1:167013212-167013631	HepG2	liver:	n/a	chr1:167013479-167013492
18	CREB1	chr1:167013285-167013685	HepG2	liver:	n/a	chr1:167013479-167013492
19	CTCF	chr1:167013578-167013584	MCF-7	breast:	n/a	n/a
20	E2F4	chr1:167015071-167015207	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr1:167013307-167013709	MCF10A-Er-Src	breast:	n/a	chr1:167013480-167013489 chr1:167013482-167013491
22	E2F6	chr1:167013320-167013628	K562	blood:	n/a	chr1:167013480-167013489 chr1:167013482-167013491
23	ELF1	chr1:167013234-167013608	A549	lung:	n/a	chr1:167013441-167013450
24	ELF1	chr1:167013195-167013698	MCF-7	breast:	n/a	chr1:167013441-167013450
25	ELF1	chr1:167012982-167013696	K562	blood:	n/a	chr1:167013441-167013450
26	ELF1	chr1:167013291-167013560	HepG2	liver:	n/a	chr1:167013441-167013450
27	ELF1	chr1:167013238-167013651	HepG2	liver:	n/a	chr1:167013441-167013450
28	ELF1	chr1:167013118-167013702	GM12878	blood:	n/a	chr1:167013441-167013450
29	ELF1	chr1:167013158-167013661	GM12878	blood:	n/a	chr1:167013441-167013450
30	ELF1	chr1:167013214-167013718	K562	blood:	n/a	chr1:167013441-167013450
31	ELF1	chr1:167012996-167013748	MCF-7	breast:	n/a	chr1:167013441-167013450
32	ELK1	chr1:167013298-167013479	GM12878	blood:	n/a	n/a
33	ELK1	chr1:167013313-167013467	K562	blood:	n/a	n/a
34	EP300	chr1:167013235-167013656	K562	blood:	n/a	n/a
35	FAM48A	chr1:167011424-167011482	GM12878	blood:	n/a	n/a
36	FOS	chr1:167013392-167013617	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr1:167013400-167013558	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr1:167013409-167013567	MCF10A-Er-Src	breast:	n/a	n/a
39	FOXA1	chr1:167013377-167013674	T-47D	breast:	n/a	n/a
40	GABPA	chr1:167013329-167013587	K562	blood:	n/a	n/a
41	GABPA	chr1:167013192-167013634	MCF-7	breast:	n/a	n/a
42	GABPA	chr1:167013299-167013683	K562	blood:	n/a	n/a
43	GATA2	chr1:167004069-167004173	SH-SY5Y	brain:	n/a	n/a
44	HA-E2F1	chr1:167013074-167013836	MCF-7	breast:	n/a	chr1:167013480-167013489 chr1:167013482-167013491
45	HCFC1	chr1:167013310-167013615	K562	blood:	n/a	n/a
46	HEY1	chr1:167013255-167013612	K562	blood:	n/a	chr1:167013482-167013491
47	HMGN3	chr1:167013358-167013592	K562	blood:	n/a	n/a
48	IRF1	chr1:167013453-167013560	K562	blood:	n/a	n/a
49	JUN	chr1:167012841-167013753	K562	blood:	n/a	n/a
50	JUN	chr1:167013341-167013638	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:167013332-167013382	Jurkat	blood:	n/a
2	chr1:167013332-167013382	HNPCEpiC	eye:	n/a
3	chr1:167013332-167013382	LNCaP	prostate:	n/a
4	chr1:167013332-167013382	IMR90	lung:	fetal
5	chr1:167013332-167013382	NHDF-neo	bronchial:	n/a
6	chr1:167013332-167013382	NT2-D1	testis:	n/a
7	chr1:167013332-167013382	GM12892	blood:	n/a
8	chr1:167013332-167013382	AG09319	gingival:	n/a
9	chr1:167013332-167013382	HRCEpiC	kidney:	n/a
10	chr1:167013332-167013382	AoSMC	blood vessel:	n/a
11	chr1:167013332-167013382	ProgFib	skin:	n/a
12	chr1:167013332-167013382	HepG2	liver:	n/a
13	chr1:167013332-167013382	HRPEpiC	eye:	n/a
14	chr1:167013332-167013382	AG04450	lung:	fetal
15	chr1:167013332-167013382	SAEC	small airway:	n/a
16	chr1:167013332-167013382	K562	blood:	n/a
17	chr1:167013332-167013382	PrEC	prostate:	n/a
18	chr1:167013332-167013382	HCT-116	colon:	n/a
19	chr1:167013332-167013382	HAEpiC	amniotic membrane:	n/a
20	chr1:167013332-167013382	HL-60	blood:	n/a
21	chr1:167013332-167013382	HCPEpiC	choroid plexus:	n/a
22	chr1:167013332-167013382	ovcar-3	ovarian:	n/a
23	chr1:167013332-167013382	U87	brain:	n/a
24	chr1:167013332-167013382	GM12878	blood:	n/a
25	chr1:167013332-167013382	SK-N-SH_RA	brain:	n/a
26	chr1:167013332-167013382	T-47D	breast:	n/a
27	chr1:167013332-167013382	HEEpiC	esophagus:	n/a
28	chr1:167013332-167013382	SKMC	muscle:	n/a
29	chr1:167013332-167013382	NH-A	brain:	n/a
30	chr1:167013332-167013382	Caco-2	colon:	n/a
31	chr1:167013332-167013382	AG04449	skin:	fetal
32	chr1:167013332-167013382	AG10803	skin:	n/a
33	chr1:167013332-167013382	SK-N-SH	brain:	n/a
34	chr1:167013332-167013382	H1-hESC	embryonic stem cell:	embryo
35	chr1:167013332-167013382	Hela-S3	cervix:	n/a
36	chr1:167013332-167013382	A549	lung:	n/a
37	chr1:167013332-167013382	HCF	heart:	n/a
38	chr1:167013332-167013382	NHBE	bronchial:	n/a
39	chr1:167013332-167013382	PANC-1	pancreas:	n/a
40	chr1:167013332-167013382	HMEC	breast:	n/a
41	chr1:167013332-167013382	HCM	heart:	n/a
42	chr1:167013332-167013382	PFSK-1	brain:	n/a
43	chr1:167013332-167013382	NB4	blood:	n/a
44	chr1:167013332-167013382	GM19239	blood:	n/a
45	chr1:167013332-167013382	MCF-7	breast:	n/a
46	chr1:167013332-167013382	HUVEC	blood vessel:	n/a
47	chr1:167013332-167013382	BE2_C	brain:	n/a
48	chr1:167013332-167013382	CMK	blood:	n/a
49	chr1:167013332-167013382	MCF10A-Er-Src	breast:	n/a
50	chr1:167013332-167013382	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:166806409..166808484-chr1:167002328..167004286,2	K562	blood:
2	chr1:166807506..166810186-chr1:167012787..167014455,2	MCF-7	breast:
3	chr1:167012979..167014978-chr1:167017542..167019812,2	K562	blood:
4	chr1:167002101..167004859-chr1:167007151..167009265,2	MCF-7	breast:
5	chr1:166844981..166846791-chr1:167011977..167013580,2	MCF-7	breast:
6	chr1:167009577..167010118-chr1:167021584..167022369,2	MCF-7	breast:
7	chr1:167002101..167004859-chr1:167007151..167009265,2	MCF-7	breast:
8	chr1:167012456..167017091-chr1:167019887..167022128,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPA33-2	chr1:167010187-167010352	NONHSAT007377

Variant related genes	Relation type
ENSG00000238325	TF binding region
ENSG00000238325	CpG island
ENSG00000227907	chromatin interactions
ENSG00000152382	chromatin interactions
ENSG00000143157	chromatin interactions

Extended variants
information (count: 185 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:185 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7555095	chr1:167003539-167003540	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562770809	chr1:167003576-167003577	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs2225153	chr1:167003579-167003580	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs376102587	chr1:167003595-167003596	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs374320955	chr1:167003672-167003673	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs147673593	chr1:167003674-167003675	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs527767086	chr1:167003689-167003690	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs148337037	chr1:167003743-167003744	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs578218821	chr1:167003816-167003817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567496235	chr1:167003830-167003831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs55728917	chr1:167003843-167003844	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs4657620	chr1:167003861-167003862	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs182610997	chr1:167003872-167003873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538965679	chr1:167003885-167003886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4657621	chr1:167003894-167003895	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs138641756	chr1:167003949-167003950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186658324	chr1:167003972-167003973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533851838	chr1:167004012-167004013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142318372	chr1:167004046-167004047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573671293	chr1:167004091-167004092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192588576	chr1:167004123-167004124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184829864	chr1:167004188-167004189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143293660	chr1:167004195-167004196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544940838	chr1:167004226-167004227	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs560096673	chr1:167004300-167004301	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs572134291	chr1:167004302-167004303	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs559193685	chr1:167004356-167004357	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs542631468	chr1:167004401-167004402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561661538	chr1:167004472-167004473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531720057	chr1:167004510-167004511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550302430	chr1:167004516-167004517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528244426	chr1:167004537-167004538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189211912	chr1:167004560-167004561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532826589	chr1:167004590-167004591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548139332	chr1:167004594-167004595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs199806865	chr1:167004605-167004606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116269775	chr1:167004613-167004614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs72689351	chr1:167004647-167004648	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs367846246	chr1:167004710-167004711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148335080	chr1:167004785-167004786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569288195	chr1:167009621-167009622	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs375392681	chr1:167009623-167009624	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs551551960	chr1:167009634-167009635	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs567614034	chr1:167009725-167009726	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs559226122	chr1:167009726-167009727	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs376716013	chr1:167009746-167009747	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs191750368	chr1:167009777-167009778	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs534202356	chr1:167009801-167009802	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573989440	chr1:167009814-167009815	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs148963429	chr1:167009816-167009817	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	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
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
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
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	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
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD

Chromatin state (count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:167002800-167003600	Enhancers	Liver	Liver
2	chr1:167003400-167003800	Flanking Active TSS	Fetal Heart	heart
3	chr1:167003800-167004200	Enhancers	Fetal Heart	heart
4	chr1:167004200-167004400	Flanking Active TSS	Fetal Heart	heart
5	chr1:167004400-167004800	Enhancers	Fetal Heart	heart
6	chr1:167012200-167012800	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr1:167012200-167012800	Enhancers	Thymus	Thymus
8	chr1:167012200-167013000	Enhancers	Primary B cells from peripheral blood	blood
9	chr1:167012200-167013800	Active TSS	Breast Myoepithelial Primary Cells	Breast
10	chr1:167012400-167012600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
11	chr1:167012400-167012800	Enhancers	Primary B cells from cord blood	blood
12	chr1:167012400-167012800	Enhancers	Primary T cells fromperipheralblood	blood
13	chr1:167012400-167012800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr1:167012400-167013000	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr1:167012400-167013000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr1:167012400-167013000	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr1:167012400-167013000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr1:167012400-167013000	Enhancers	Colon Smooth Muscle	Colon
19	chr1:167012400-167013000	Enhancers	Fetal Thymus	thymus
20	chr1:167012600-167012800	Enhancers	Primary T cells from cord blood	blood
21	chr1:167012600-167012800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr1:167012600-167012800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:167012600-167012800	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr1:167012600-167012800	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr1:167012600-167012800	Enhancers	Dnd41	blood
26	chr1:167012600-167012800	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr1:167012600-167013000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr1:167012600-167013000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr1:167012600-167013000	Enhancers	Colonic Mucosa	Colon
30	chr1:167012600-167013200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
31	chr1:167012800-167013000	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr1:167012800-167013000	Enhancers	Primary hematopoietic stem cells	blood
33	chr1:167012800-167013000	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
34	chr1:167012800-167013000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:167012800-167013000	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr1:167012800-167013000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr1:167012800-167013000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr1:167012800-167013000	Enhancers	Liver	Liver
39	chr1:167012800-167013000	Enhancers	Brain Hippocampus Middle	brain
40	chr1:167012800-167013000	Enhancers	Rectal Smooth Muscle	rectum
41	chr1:167012800-167013000	Flanking Active TSS	Thymus	Thymus
42	chr1:167012800-167013200	Active TSS	Primary T cells fromperipheralblood	blood
43	chr1:167012800-167013200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr1:167012800-167013200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
45	chr1:167012800-167013400	Flanking Active TSS	Primary B cells from cord blood	blood
46	chr1:167012800-167013400	Flanking Active TSS	Primary T cells from cord blood	blood
47	chr1:167012800-167013400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr1:167012800-167013800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr1:167012800-167013800	Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr1:167012800-167013800	Active TSS	Rectal Mucosa Donor 29	rectum

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