Variant report

Variant	esv1813216
Chromosome Location	chr1:224079049-224138188
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:741)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:224124412-224124623	K562	blood:	n/a	n/a
2	ARID3A	chr1:224119208-224119671	K562	blood:	n/a	n/a
3	ATF1	chr1:224119207-224119478	K562	blood:	n/a	n/a
4	BATF	chr1:224104058-224104261	GM12878	blood:	n/a	n/a
5	BATF	chr1:224108555-224108855	GM12878	blood:	n/a	chr1:224108835-224108844
6	BATF	chr1:224095793-224096047	GM12878	blood:	n/a	n/a
7	BATF	chr1:224103998-224104234	GM12878	blood:	n/a	n/a
8	BATF	chr1:224092998-224093284	GM12878	blood:	n/a	n/a
9	BATF	chr1:224108598-224108877	GM12878	blood:	n/a	chr1:224108835-224108844
10	BATF	chr1:224100112-224100738	GM12878	blood:	n/a	chr1:224100431-224100442
11	BATF	chr1:224100132-224100691	GM12878	blood:	n/a	chr1:224100431-224100442
12	BCL11A	chr1:224108051-224108199	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:224083605-224083817	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:224095758-224096028	GM12878	blood:	n/a	n/a
15	BCL11A	chr1:224093639-224093850	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:224103937-224104270	GM12878	blood:	n/a	chr1:224104160-224104168
17	BCL11A	chr1:224090921-224091109	GM12878	blood:	n/a	chr1:224091090-224091098
18	BCL11A	chr1:224091435-224091635	GM12878	blood:	n/a	chr1:224091454-224091463
19	BCL11A	chr1:224100121-224100579	GM12878	blood:	n/a	chr1:224100434-224100443
20	BCL11A	chr1:224100059-224100720	GM12878	blood:	n/a	chr1:224100434-224100443
21	BCL11A	chr1:224095804-224096023	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:224094248-224094435	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:224111240-224111434	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:224110721-224110974	HepG2	liver:	n/a	n/a
25	BHLHE40	chr1:224108563-224108836	HepG2	liver:	n/a	n/a
26	BHLHE40	chr1:224112070-224112315	HepG2	liver:	n/a	n/a
27	CCNT2	chr1:224119307-224119476	K562	blood:	n/a	n/a
28	CCNT2	chr1:224124418-224124640	K562	blood:	n/a	n/a
29	CEBPB	chr1:224119272-224119685	K562	blood:	n/a	n/a
30	CEBPB	chr1:224111522-224111543	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:224128087-224128547	K562	blood:	n/a	n/a
32	CEBPB	chr1:224119050-224119660	K562	blood:	n/a	n/a
33	CEBPD	chr1:224124238-224124681	K562	blood:	n/a	n/a
34	CEBPD	chr1:224119236-224119796	K562	blood:	n/a	n/a
35	CEBPD	chr1:224123228-224123626	K562	blood:	n/a	n/a
36	CHD2	chr1:224123348-224123652	K562	blood:	n/a	n/a
37	CTCF	chr1:224095866-224096036	GM12892	blood:	n/a	chr1:224095905-224095912
38	CTCF	chr1:224108580-224108730	GM12868	blood:	n/a	n/a
39	CTCF	chr1:224108580-224108730	BE2_C	brain:	n/a	n/a
40	CTCF	chr1:224108820-224108970	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr1:224095822-224096039	MCF-7	breast:	n/a	chr1:224095905-224095912
42	CTCF	chr1:224095740-224095890	NHEK	skin:	n/a	n/a
43	CTCF	chr1:224095740-224095890	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr1:224095720-224095870	AG04450	lung:	n/a	n/a
45	CTCF	chr1:224095792-224096063	A549	lung:	n/a	chr1:224095905-224095912
46	CTCF	chr1:224119327-224119523	K562	blood:	n/a	n/a
47	CTCF	chr1:224088120-224088270	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr1:224095720-224095870	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr1:224108580-224108730	A549	lung:	n/a	n/a
50	CTCF	chr1:224088006-224088078	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:224133090-224133140	HNPCEpiC	eye:	n/a
2	chr1:224133090-224133140	HL-60	blood:	n/a
3	chr1:224133090-224133140	GM06990	blood:	n/a
4	chr1:224136349-224136399	HAEpiC	amniotic membrane:	n/a
5	chr1:224136349-224136399	SKMC	muscle:	n/a
6	chr1:224133090-224133140	NB4	blood:	n/a
7	chr1:224133090-224133140	HRCEpiC	kidney:	n/a
8	chr1:224133090-224133140	HMEC	breast:	n/a
9	chr1:224133090-224133140	HEK293	kidney:	embryo
10	chr1:224133090-224133140	T-47D	breast:	n/a
11	chr1:224136349-224136399	CMK	blood:	n/a
12	chr1:224136349-224136399	GM12892	blood:	n/a
13	chr1:224133090-224133140	HUVEC	blood vessel:	n/a
14	chr1:224136349-224136399	HUVEC	blood vessel:	n/a
15	chr1:224136349-224136399	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:224136349-224136399	GM19239	blood:	n/a
17	chr1:224136349-224136399	AG09309	skin:	n/a
18	chr1:224133090-224133140	ECC-1	luminal epithelium:	n/a
19	chr1:224133090-224133140	Caco-2	colon:	n/a
20	chr1:224136349-224136399	HIPEpiC	eye:	n/a
21	chr1:224133090-224133140	AG09309	skin:	n/a
22	chr1:224133090-224133140	HIPEpiC	eye:	n/a
23	chr1:224133090-224133140	GM19239	blood:	n/a
24	chr1:224133090-224133140	K562	blood:	n/a
25	chr1:224136349-224136399	AG10803	skin:	n/a
26	chr1:224136349-224136399	ovcar-3	ovarian:	n/a
27	chr1:224136349-224136399	HRCEpiC	kidney:	n/a
28	chr1:224133090-224133140	LNCaP	prostate:	n/a
29	chr1:224133090-224133140	NHDF-neo	bronchial:	n/a
30	chr1:224133090-224133140	NT2-D1	testis:	n/a
31	chr1:224133090-224133140	ProgFib	skin:	n/a
32	chr1:224133090-224133140	HEEpiC	esophagus:	n/a
33	chr1:224133090-224133140	NHBE	bronchial:	n/a
34	chr1:224136349-224136399	HEK293	kidney:	embryo
35	chr1:224133090-224133140	MCF10A-Er-Src	breast:	n/a
36	chr1:224136349-224136399	PrEC	prostate:	n/a
37	chr1:224136349-224136399	AG04449	skin:	fetal
38	chr1:224136349-224136399	BJ	skin:	n/a
39	chr1:224136349-224136399	Jurkat	blood:	n/a
40	chr1:224133090-224133140	RPTEC	kidney:	n/a
41	chr1:224133090-224133140	CMK	blood:	n/a
42	chr1:224133090-224133140	GM12891	blood:	n/a
43	chr1:224136349-224136399	RPTEC	kidney:	n/a
44	chr1:224136349-224136399	NT2-D1	testis:	n/a
45	chr1:224133090-224133140	SK-N-SH	brain:	n/a
46	chr1:224133090-224133140	IMR90	lung:	fetal
47	chr1:224136349-224136399	GM12878	blood:	n/a
48	chr1:224133090-224133140	H1-hESC	embryonic stem cell:	embryo
49	chr1:224136349-224136399	MCF-7	breast:	n/a
50	chr1:224133090-224133140	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:223900030..223900536-chr1:224108678..224109196,2	K562	blood:
2	chr1:224030638..224033175-chr1:224122761..224125405,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PARP1-3	chr1:224098433-224099085	expRegAs_chr1_21128_-
2	lnc-PARP1-4	chr1:224096672-224097019	expRegAs_chr1_21127_-

No data

Variant related genes	Relation type
CICP5	TF binding region
CICP5	CpG island
ENSG00000162909	chromatin interactions

Extended variants
information (count: 668 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:668 , 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	rs10915956	chr1:224079049-224079050	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115995153	chr1:224079103-224079104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558003319	chr1:224079127-224079128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573180074	chr1:224079145-224079146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199771250	chr1:224079147-224079148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs58391315	chr1:224079182-224079183	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs12032261	chr1:224079183-224079184	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs114442862	chr1:224079190-224079191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12037320	chr1:224079237-224079238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562981925	chr1:224079290-224079291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534023378	chr1:224079309-224079310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533269781	chr1:224079339-224079340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533332197	chr1:224079378-224079379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs59650778	chr1:224079391-224079392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560498093	chr1:224079502-224079503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148831386	chr1:224079560-224079561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537095151	chr1:224079610-224079611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546618178	chr1:224079680-224079681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs3911756	chr1:224079689-224079690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568240194	chr1:224079709-224079710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551042492	chr1:224079716-224079717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143595218	chr1:224079718-224079719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6703817	chr1:224079763-224079764	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs568624646	chr1:224079765-224079766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539177095	chr1:224079794-224079795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550949204	chr1:224079796-224079797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566173678	chr1:224079828-224079829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140980170	chr1:224079829-224079830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566688627	chr1:224079862-224079863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112990434	chr1:224079882-224079883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144781964	chr1:224079910-224079911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138846363	chr1:224079923-224079924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185825213	chr1:224079932-224079933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6604732	chr1:224079934-224079935	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs575169091	chr1:224079952-224079953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs60769544	chr1:224079970-224079971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12736521	chr1:224079992-224079993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557813012	chr1:224080052-224080053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs3958207	chr1:224080080-224080081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201886952	chr1:224080083-224080084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs3992815	chr1:224080090-224080091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545552355	chr1:224080173-224080174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs3992793	chr1:224080197-224080198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs3992794	chr1:224080207-224080208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560487895	chr1:224080295-224080296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572392681	chr1:224080308-224080309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200112209	chr1:224080329-224080330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561842482	chr1:224080351-224080352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4653421	chr1:224080380-224080381	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs550482013	chr1:224080382-224080383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Cancer	17060936	CNVD
Ewing''s sarcoma	19144156	CNVD

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224074400-224079200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:224077400-224085600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:224079200-224079400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:224079200-224079400	Enhancers	Liver	Liver
5	chr1:224083800-224084000	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr1:224084000-224084800	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr1:224084000-224085600	Weak transcription	Fetal Muscle Leg	muscle
8	chr1:224084800-224085000	Enhancers	Psoas Muscle	Psoas
9	chr1:224084800-224086400	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr1:224085000-224086000	Weak transcription	Psoas Muscle	Psoas
11	chr1:224085400-224087400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:224085600-224086200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:224086000-224086400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:224086000-224086400	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr1:224086000-224086400	Enhancers	Psoas Muscle	Psoas
16	chr1:224086000-224086400	Enhancers	NHDF-Ad	bronchial
17	chr1:224086200-224087600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr1:224087600-224087800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:224087600-224087800	Enhancers	Fetal Muscle Leg	muscle
20	chr1:224094400-224094600	Enhancers	Fetal Thymus	thymus
21	chr1:224094400-224095200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr1:224094600-224095600	Weak transcription	Fetal Thymus	thymus
23	chr1:224095600-224096200	Enhancers	Fetal Thymus	thymus
24	chr1:224096000-224096200	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr1:224096200-224097400	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr1:224097400-224099600	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr1:224097800-224099000	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr1:224099000-224100600	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr1:224099600-224101600	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr1:224100600-224102000	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr1:224101600-224102000	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr1:224119200-224119600	Enhancers	K562	blood
33	chr1:224135800-224149800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:224136200-224139400	Weak transcription	Fetal Intestine Small	intestine
35	chr1:224136400-224179800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr1:224136600-224149200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr1:224137200-224138600	Weak transcription	Fetal Stomach	stomach
38	chr1:224137600-224139200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:224137800-224139400	Weak transcription	Adipose Nuclei	Adipose
40	chr1:224137800-224139400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr1:224137800-224139400	Weak transcription	Fetal Muscle Trunk	muscle
42	chr1:224137800-224139400	Weak transcription	Placenta	Placenta
43	chr1:224137800-224139400	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr1:224137800-224139400	Weak transcription	Spleen	Spleen
45	chr1:224137800-224160600	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr1:224138000-224139400	Weak transcription	Lung	lung
47	chr1:224138000-224139600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:224138000-224139600	Weak transcription	Ovary	ovary
49	chr1:224138000-224140000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr1:224138000-224141000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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