Variant report

Variant	nsv945430
Chromosome Location	chr1:246767834-246771762
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:29)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:29 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr1:246769297-246769634	K562	blood:	n/a	n/a
2	CTCF	chr1:246768877-246769064	A549	lung:	n/a	n/a
3	EP300	chr1:246771733-246772608	T-47D	breast:	n/a	chr1:246772458-246772467
4	FOXA1	chr1:246771741-246772676	T-47D	breast:	n/a	n/a
5	FOXA1	chr1:246771638-246772598	T-47D	breast:	n/a	n/a
6	FOXM1	chr1:246771657-246772712	ECC-1	luminal epithelium:	n/a	n/a
7	FOXM1	chr1:246771713-246772651	ECC-1	luminal epithelium:	n/a	n/a
8	GATA2	chr1:246769695-246770098	K562	blood:	n/a	n/a
9	GATA3	chr1:246771728-246772637	MCF-7	breast:	n/a	n/a
10	GATA3	chr1:246771718-246772661	T-47D	breast:	n/a	n/a
11	GATA3	chr1:246771656-246772640	MCF-7	breast:	n/a	n/a
12	GATA3	chr1:246771678-246772563	T-47D	breast:	n/a	n/a
13	JUND	chr1:246771740-246772652	T-47D	breast:	n/a	n/a
14	MAZ	chr1:246771695-246772629	IMR90	lung:	n/a	chr1:246772398-246772413 chr1:246772399-246772410 chr1:246772399-246772409 chr1:246772399-246772410 chr1:246772398-246772411 chr1:246772400-246772409 chr1:246772396-246772411 chr1:246772400-246772409 chr1:246772401-246772408
15	MXI1	chr1:246771486-246773035	IMR90	lung:	n/a	n/a
16	MYC	chr1:246771610-246772687	MCF10A-Er-Src	breast:	n/a	chr1:246772398-246772413 chr1:246772399-246772410 chr1:246772399-246772409 chr1:246772399-246772410 chr1:246772398-246772411 chr1:246772400-246772409 chr1:246772396-246772411 chr1:246772400-246772409 chr1:246772401-246772408
17	NR2F2	chr1:246769753-246770014	K562	blood:	n/a	n/a
18	PAX5	chr1:246768708-246769092	GM12878	blood:	n/a	n/a
19	POLR2A	chr1:246768749-246769172	GM12878	blood:	n/a	n/a
20	POLR2A	chr1:246771607-246771670	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr1:246770310-246770645	K562	blood:	n/a	n/a
22	POLR2A	chr1:246770593-246770644	MCF-7	breast:	n/a	n/a
23	POLR2A	chr1:246768807-246768813	K562	blood:	n/a	n/a
24	RCOR1	chr1:246771723-246772740	IMR90	lung:	n/a	n/a
25	SIN3AK20	chr1:246771714-246772728	MCF-7	breast:	n/a	n/a
26	SPI1	chr1:246770825-246770988	K562	blood:	n/a	n/a
27	SPI1	chr1:246768807-246768963	K562	blood:	n/a	n/a
28	TCF12	chr1:246771716-246772754	ECC-1	luminal epithelium:	n/a	chr1:246772296-246772306
29	TEAD4	chr1:246771747-246772710	ECC-1	luminal epithelium:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246770778-246770828	ECC-1	luminal epithelium:	n/a
2	chr1:246768697-246768747	HNPCEpiC	eye:	n/a
3	chr1:246770778-246770828	CMK	blood:	n/a
4	chr1:246768697-246768747	NB4	blood:	n/a
5	chr1:246770778-246770828	HRPEpiC	eye:	n/a
6	chr1:246768697-246768747	AG04449	skin:	fetal
7	chr1:246768697-246768747	PANC-1	pancreas:	n/a
8	chr1:246770778-246770828	HAEpiC	amniotic membrane:	n/a
9	chr1:246768697-246768747	A549	lung:	n/a
10	chr1:246770778-246770828	IMR90	lung:	fetal
11	chr1:246768697-246768747	NHBE	bronchial:	n/a
12	chr1:246770778-246770828	HCPEpiC	choroid plexus:	n/a
13	chr1:246768697-246768747	AoSMC	blood vessel:	n/a
14	chr1:246770778-246770828	SAEC	small airway:	n/a
15	chr1:246770778-246770828	HIPEpiC	eye:	n/a
16	chr1:246768697-246768747	NT2-D1	testis:	n/a
17	chr1:246770778-246770828	AG04449	skin:	fetal
18	chr1:246768697-246768747	HUVEC	blood vessel:	n/a
19	chr1:246770778-246770828	NT2-D1	testis:	n/a
20	chr1:246768697-246768747	IMR90	lung:	fetal
21	chr1:246768697-246768747	K562	blood:	n/a
22	chr1:246768697-246768747	GM19239	blood:	n/a
23	chr1:246770778-246770828	BJ	skin:	n/a
24	chr1:246768697-246768747	SAEC	small airway:	n/a
25	chr1:246770778-246770828	HCM	heart:	n/a
26	chr1:246770778-246770828	U87	brain:	n/a
27	chr1:246768697-246768747	ovcar-3	ovarian:	n/a
28	chr1:246770778-246770828	HL-60	blood:	n/a
29	chr1:246770778-246770828	AG10803	skin:	n/a
30	chr1:246768697-246768747	BE2_C	brain:	n/a
31	chr1:246770778-246770828	Hela-S3	cervix:	n/a
32	chr1:246768697-246768747	NH-A	brain:	n/a
33	chr1:246768697-246768747	HCT-116	colon:	n/a
34	chr1:246768697-246768747	HEK293	kidney:	embryo
35	chr1:246770778-246770828	AG09319	gingival:	n/a
36	chr1:246768697-246768747	HAEpiC	amniotic membrane:	n/a
37	chr1:246770778-246770828	HNPCEpiC	eye:	n/a
38	chr1:246768697-246768747	Hela-S3	cervix:	n/a
39	chr1:246770778-246770828	HPAEpiC	pulmonary alveolar:	n/a
40	chr1:246768697-246768747	AG10803	skin:	n/a
41	chr1:246770778-246770828	SKMC	muscle:	n/a
42	chr1:246770778-246770828	HUVEC	blood vessel:	n/a
43	chr1:246770778-246770828	BE2_C	brain:	n/a
44	chr1:246768697-246768747	HCPEpiC	choroid plexus:	n/a
45	chr1:246768697-246768747	GM06990	blood:	n/a
46	chr1:246768697-246768747	HCF	heart:	n/a
47	chr1:246768697-246768747	Caco-2	colon:	n/a
48	chr1:246770778-246770828	RPTEC	kidney:	n/a
49	chr1:246770778-246770828	Caco-2	colon:	n/a
50	chr1:246768697-246768747	CMK	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246759373..246761644-chr1:246764885..246767853,2	MCF-7	breast:
2	chr1:246770998..246772509-chr1:246887067..246889147,2	MCF-7	breast:
3	chr1:246728431..246731272-chr1:246765125..246768434,3	MCF-7	breast:
4	chr1:246765334..246768163-chr1:246769241..246772200,2	MCF-7	breast:
5	chr1:246728819..246730671-chr1:246770818..246772459,2	MCF-7	breast:
6	chr1:246765334..246768163-chr1:246769241..246772200,2	MCF-7	breast:
7	chr1:246769755..246771548-chr1:246776267..246778089,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCCPDH-2	chr1:246770913-246771404	ENSG00000225300.1
2	lnc-SCCPDH-2	chr1:246769175-246770642	ENSG00000225300.1

No data

Variant related genes	Relation type
ENSG00000225300	TF binding region
ENSG00000225300	CpG island
ENSG00000143653	chromatin interactions
ENSG00000162851	chromatin interactions
ENSG00000162852	chromatin interactions

Extended variants
information (count: 256 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:256 , 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	rs575913441	chr1:246767843-246767844	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs536380813	chr1:246767856-246767857	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs147336521	chr1:246767882-246767883	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs140976682	chr1:246767930-246767931	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs555991803	chr1:246767949-246767950	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs370398840	chr1:246767958-246767959	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs567896332	chr1:246767976-246767977	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs530400212	chr1:246767977-246767978	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs144846326	chr1:246767999-246768000	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs560516980	chr1:246768002-246768003	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs191359839	chr1:246768025-246768026	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs185558150	chr1:246768031-246768032	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs569346561	chr1:246768041-246768042	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs147921088	chr1:246768045-246768046	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs548163937	chr1:246768067-246768068	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs113087335	chr1:246768078-246768079	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs534965117	chr1:246768113-246768114	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs568158935	chr1:246768119-246768120	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs533835092	chr1:246768133-246768134	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs140067457	chr1:246768140-246768141	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs7518388	chr1:246768176-246768177	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs570512701	chr1:246768201-246768202	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs7527517	chr1:246768255-246768256	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs7532014	chr1:246768285-246768286	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs142579614	chr1:246768310-246768311	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs555959557	chr1:246768345-246768346	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs567209970	chr1:246768346-246768347	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs576185318	chr1:246768386-246768387	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs541978970	chr1:246768390-246768391	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs534537711	chr1:246768416-246768417	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs555392047	chr1:246768458-246768459	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150957502	chr1:246768484-246768485	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540523061	chr1:246768492-246768493	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560846823	chr1:246768504-246768505	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532560629	chr1:246768505-246768506	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190431959	chr1:246768527-246768528	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562966583	chr1:246768529-246768530	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7530067	chr1:246768605-246768606	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115570568	chr1:246768606-246768607	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548323550	chr1:246768621-246768622	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568069415	chr1:246768638-246768639	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7521252	chr1:246768651-246768652	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs80151139	chr1:246768662-246768663	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547340713	chr1:246768665-246768666	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140745886	chr1:246768670-246768671	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7521263	chr1:246768698-246768699	Weak transcription ZNF genes & repeats Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs181620968	chr1:246768723-246768724	Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs150077698	chr1:246768727-246768728	Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs569905462	chr1:246768729-246768730	Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs535539873	chr1:246768739-246768740	Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	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
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Oral cancer	21386901	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:157 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246739000-246806200	Weak transcription	Aorta	Aorta
2	chr1:246744400-246770800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr1:246747400-246772000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr1:246748000-246771600	Weak transcription	Hela-S3	cervix
5	chr1:246748600-246770200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:246749000-246772000	Weak transcription	Small Intestine	intestine
7	chr1:246751200-246772000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr1:246751200-246772200	Weak transcription	Brain Substantia Nigra	brain
9	chr1:246753600-246771800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr1:246753800-246768400	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr1:246755200-246772000	Weak transcription	Spleen	Spleen
12	chr1:246755400-246832800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr1:246756200-246774000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr1:246757400-246771800	Weak transcription	HSMMtube	muscle
15	chr1:246757600-246772200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:246758800-246771800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:246759200-246771800	Weak transcription	Liver	Liver
18	chr1:246761000-246771800	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr1:246761200-246770200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr1:246761200-246771600	Weak transcription	HepG2	liver
21	chr1:246761200-246771600	Weak transcription	Osteobl	bone
22	chr1:246761200-246772000	Weak transcription	Gastric	stomach
23	chr1:246761400-246771800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:246761400-246771800	Weak transcription	NHEK	skin
25	chr1:246761400-246772000	Weak transcription	Primary B cells from peripheral blood	blood
26	chr1:246761400-246772000	Weak transcription	Duodenum Mucosa	Duodenum
27	chr1:246761600-246771800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:246762200-246771000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr1:246762800-246771800	Weak transcription	Ovary	ovary
30	chr1:246762800-246771800	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr1:246762800-246771800	Weak transcription	Rectal Smooth Muscle	rectum
32	chr1:246763000-246771000	Weak transcription	Right Atrium	heart
33	chr1:246763000-246771800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr1:246763400-246768600	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr1:246763400-246770800	Weak transcription	Lung	lung
36	chr1:246763600-246771800	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr1:246764200-246771800	Weak transcription	Esophagus	oesophagus
38	chr1:246764200-246784200	Weak transcription	Thymus	Thymus
39	chr1:246765800-246771800	Weak transcription	Right Ventricle	heart
40	chr1:246765800-246779600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr1:246766000-246768800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:246766000-246770800	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr1:246766000-246770800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr1:246766000-246770800	Weak transcription	Psoas Muscle	Psoas
45	chr1:246766000-246771600	Weak transcription	NHLF	lung
46	chr1:246766000-246771800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr1:246766000-246771800	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr1:246766000-246772000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr1:246766200-246770800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr1:246766200-246770800	Weak transcription	Primary T helper cells fromperipheralblood	blood

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