Variant report

Variant	nsv872588
Chromosome Location	chr1:185081903-185117688
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:79)
CpG islands
(count:61)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:79 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:185101766-185101912	HepG2	liver:	n/a	n/a
2	ATF1	chr1:185092894-185092953	K562	blood:	n/a	n/a
3	CBX3	chr1:185101692-185102077	K562	blood:	n/a	n/a
4	CBX3	chr1:185101681-185102056	K562	blood:	n/a	n/a
5	CBX3	chr1:185101746-185102081	HCT-116	colon:	n/a	n/a
6	CEBPB	chr1:185090910-185091097	A549	lung:	n/a	n/a
7	CEBPB	chr1:185083290-185083460	HepG2	liver:	n/a	chr1:185083324-185083335
8	CEBPB	chr1:185083280-185083479	K562	blood:	n/a	chr1:185083324-185083335
9	CEBPB	chr1:185090845-185091053	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:185114410-185114717	K562	blood:	n/a	chr1:185114557-185114568 chr1:185114555-185114568 chr1:185114555-185114568
11	CEBPB	chr1:185101948-185102274	HepG2	liver:	n/a	chr1:185102093-185102104
12	CHD2	chr1:185087093-185087197	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr1:185102781-185102868	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr1:185095480-185095522	MCF-7	breast:	n/a	n/a
15	CTCF	chr1:185091864-185091951	Fibrobl	skin:	n/a	n/a
16	CTCF	chr1:185084410-185084466	ProgFib	skin:	n/a	n/a
17	FOS	chr1:185113442-185113676	MCF10A-Er-Src	breast:	n/a	n/a
18	FOSL2	chr1:185113298-185113882	SK-N-SH	brain:	n/a	n/a
19	GATA1	chr1:185106920-185107462	PBDE	blood:	n/a	chr1:185106960-185106969 chr1:185107211-185107232 chr1:185107109-185107119
20	GATA1	chr1:185108195-185108829	PBDE	blood:	n/a	chr1:185108376-185108385 chr1:185108373-185108389 chr1:185108378-185108385 chr1:185108371-185108392 chr1:185108376-185108386 chr1:185108373-185108389 chr1:185108378-185108388
21	GATA3	chr1:185102018-185102123	SH-SY5Y	brain:	n/a	n/a
22	GATA3	chr1:185113219-185113926	SK-N-SH	brain:	n/a	n/a
23	GATA3	chr1:185081860-185082243	SH-SY5Y	brain:	n/a	n/a
24	IRF1	chr1:185114428-185114596	K562	blood:	n/a	n/a
25	IRF1	chr1:185109136-185109159	K562	blood:	n/a	n/a
26	JUN	chr1:185087868-185087917	K562	blood:	n/a	n/a
27	JUND	chr1:185113313-185113872	SK-N-SH	brain:	n/a	n/a
28	JUND	chr1:185082424-185082438	HepG2	liver:	n/a	n/a
29	JUND	chr1:185098927-185099196	HepG2	liver:	n/a	n/a
30	KAP1	chr1:185101642-185102355	K562	blood:	n/a	n/a
31	MAFF	chr1:185107403-185107635	HepG2	liver:	n/a	chr1:185107468-185107486
32	MAFK	chr1:185107389-185107579	IMR90	lung:	n/a	chr1:185107470-185107486 chr1:185107470-185107481 chr1:185107470-185107485 chr1:185107470-185107481 chr1:185107469-185107483
33	MAFK	chr1:185089756-185089921	HepG2	liver:	n/a	chr1:185089818-185089833
34	MAFK	chr1:185107369-185107561	HepG2	liver:	n/a	chr1:185107470-185107486 chr1:185107470-185107481 chr1:185107470-185107485 chr1:185107470-185107481 chr1:185107469-185107483
35	MAFK	chr1:185097884-185097897	H1-hESC	embryonic stem cell:	n/a	n/a
36	MAFK	chr1:185089787-185089953	IMR90	lung:	n/a	chr1:185089818-185089833
37	MAFK	chr1:185107351-185107654	HepG2	liver:	n/a	chr1:185107470-185107486 chr1:185107470-185107481 chr1:185107470-185107485 chr1:185107470-185107481 chr1:185107469-185107483
38	MAFK	chr1:185089739-185089946	HepG2	liver:	n/a	chr1:185089818-185089833
39	MAZ	chr1:185088025-185088038	HepG2	liver:	n/a	n/a
40	MEF2A	chr1:185113217-185113790	SK-N-SH	brain:	n/a	chr1:185113272-185113287 chr1:185113272-185113287
41	MXI1	chr1:185104840-185104940	GM12878	blood:	n/a	n/a
42	PBX3	chr1:185113281-185113829	SK-N-SH	brain:	n/a	n/a
43	POLR2A	chr1:185087560-185087629	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr1:185102401-185102437	GM12878	blood:	n/a	n/a
45	POLR2A	chr1:185084485-185084497	MCF-7	breast:	n/a	n/a
46	POLR2A	chr1:185085493-185086711	K562	blood:	n/a	n/a
47	POLR2A	chr1:185084416-185084511	Gliobla	brain:	n/a	n/a
48	POLR2A	chr1:185094463-185094520	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr1:185084416-185084435	MCF-7	breast:	n/a	n/a
50	POLR2A	chr1:185095481-185095538	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:185113945-185113995	HRPEpiC	eye:	n/a
2	chr1:185113945-185113995	HCM	heart:	n/a
3	chr1:185113945-185113995	SKMC	muscle:	n/a
4	chr1:185113945-185113995	HMEC	breast:	n/a
5	chr1:185113945-185113995	SK-N-SH_RA	brain:	n/a
6	chr1:185113945-185113995	NHBE	bronchial:	n/a
7	chr1:185113945-185113995	HUVEC	blood vessel:	n/a
8	chr1:185113945-185113995	HCT-116	colon:	n/a
9	chr1:185113945-185113995	HRE	kidney:	n/a
10	chr1:185113945-185113995	HNPCEpiC	eye:	n/a
11	chr1:185113945-185113995	SK-N-SH	brain:	n/a
12	chr1:185113945-185113995	Hepatocyte	liver:	n/a
13	chr1:185113945-185113995	Jurkat	blood:	n/a
14	chr1:185113945-185113995	BJ	skin:	n/a
15	chr1:185113945-185113995	GM06990	blood:	n/a
16	chr1:185113945-185113995	ovcar-3	ovarian:	n/a
17	chr1:185113945-185113995	BE2_C	brain:	n/a
18	chr1:185113945-185113995	HAEpiC	amniotic membrane:	n/a
19	chr1:185113945-185113995	K562	blood:	n/a
20	chr1:185113945-185113995	PFSK-1	brain:	n/a
21	chr1:185113945-185113995	T-47D	breast:	n/a
22	chr1:185113945-185113995	GM12891	blood:	n/a
23	chr1:185113945-185113995	AG10803	skin:	n/a
24	chr1:185113945-185113995	ProgFib	skin:	n/a
25	chr1:185113945-185113995	RPTEC	kidney:	n/a
26	chr1:185113945-185113995	GM12892	blood:	n/a
27	chr1:185113945-185113995	MCF-7	breast:	n/a
28	chr1:185113945-185113995	HepG2	liver:	n/a
29	chr1:185113945-185113995	ECC-1	luminal epithelium:	n/a
30	chr1:185113945-185113995	U87	brain:	n/a
31	chr1:185113945-185113995	NT2-D1	testis:	n/a
32	chr1:185113945-185113995	SAEC	small airway:	n/a
33	chr1:185113945-185113995	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:185113945-185113995	SK-N-MC	brain:	n/a
35	chr1:185113945-185113995	H1-hESC	embryonic stem cell:	embryo
36	chr1:185113945-185113995	MCF10A-Er-Src	breast:	n/a
37	chr1:185113945-185113995	GM12878	blood:	n/a
38	chr1:185113945-185113995	HEEpiC	esophagus:	n/a
39	chr1:185113945-185113995	CMK	blood:	n/a
40	chr1:185113945-185113995	HEK293	kidney:	embryo
41	chr1:185113945-185113995	Caco-2	colon:	n/a
42	chr1:185113945-185113995	Hela-S3	cervix:	n/a
43	chr1:185113945-185113995	IMR90	lung:	fetal
44	chr1:185113945-185113995	HIPEpiC	eye:	n/a
45	chr1:185113945-185113995	A549	lung:	n/a
46	chr1:185113945-185113995	AoSMC	blood vessel:	n/a
47	chr1:185113945-185113995	HCF	heart:	n/a
48	chr1:185113945-185113995	HL-60	blood:	n/a
49	chr1:185113945-185113995	AG04449	skin:	fetal
50	chr1:185113945-185113995	HCPEpiC	choroid plexus:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:185082822..185085322-chr1:185089321..185090884,2	K562	blood:
2	chr1:185113029..185115978-chr1:185116966..185118773,2	K562	blood:
3	chr1:185116622..185122065-chr1:185122168..185128175,9	MCF-7	breast:
4	chr1:185097589..185099200-chr1:185100580..185102267,2	K562	blood:
5	chr1:185104278..185107115-chr1:185121320..185123089,2	K562	blood:
6	chr1:185110219..185112548-chr1:185124480..185127523,3	MCF-7	breast:
7	chr1:185097360..185099907-chr1:185110020..185112748,3	K562	blood:
8	chr1:185093263..185096920-chr1:185097304..185100679,5	K562	blood:
9	chr1:185085659..185087885-chr1:185092859..185095086,2	K562	blood:
10	chr1:185114176..185116855-chr1:185120494..185122664,2	K562	blood:
11	chr1:185087227..185089140-chr1:185125216..185126915,2	MCF-7	breast:
12	chr1:185111010..185114000-chr1:185116930..185118963,2	MCF-7	breast:
13	chr1:185093263..185095350-chr1:185097304..185099171,2	K562	blood:
14	chr1:185099798..185103088-chr1:185104012..185107773,3	K562	blood:
15	chr1:185035986..185038971-chr1:185111907..185115590,3	MCF-7	breast:
16	chr1:185014410..185016846-chr1:185107860..185109945,2	K562	blood:
17	chr1:185013037..185015967-chr1:185083615..185085714,3	K562	blood:
18	chr1:185079216..185081191-chr1:185086441..185087955,2	K562	blood:
19	chr1:185086646..185088297-chr1:185088839..185091259,2	K562	blood:
20	chr1:185111010..185114000-chr1:185116930..185118963,2	MCF-7	breast:
21	chr1:185091571..185094298-chr1:185128377..185130619,2	K562	blood:
22	chr1:185112945..185115248-chr1:185120909..185123637,2	MCF-7	breast:
23	chr1:185014401..185016308-chr1:185117123..185120089,2	MCF-7	breast:
24	chr1:185083544..185086081-chr1:185099831..185101726,2	MCF-7	breast:
25	chr1:185097360..185099907-chr1:185110020..185112748,3	K562	blood:
26	chr1:185099798..185103088-chr1:185104012..185107773,3	K562	blood:
27	chr1:185083544..185086081-chr1:185099831..185101726,2	MCF-7	breast:
28	chr1:185113029..185115978-chr1:185116966..185118773,2	K562	blood:
29	chr1:185113319..185116352-chr1:185124187..185127216,4	MCF-7	breast:
30	chr1:185097589..185099200-chr1:185100580..185102267,2	K562	blood:
31	chr1:185093263..185095350-chr1:185097304..185099171,2	K562	blood:
32	chr1:185112895..185116881-chr1:185123287..185126781,5	K562	blood:
33	chr1:185093263..185096920-chr1:185097304..185100679,5	K562	blood:
34	chr1:185085659..185087885-chr1:185092859..185095086,2	K562	blood:
35	chr1:185115388..185115967-chr12:81272400..81273262,2	MCF-7	breast:
36	chr1:185114068..185116270-chr1:185124385..185126877,5	MCF-7	breast:

No data

Variant related genes	Relation type
TRMT1L	TF binding region
TRMT1L	CpG island
ENSG00000116668	chromatin interactions
ENSG00000121486	chromatin interactions
ENSG00000121481	chromatin interactions

Extended variants
information (count: 1206 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1206 , 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	rs10911678	chr1:185081903-185081904	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558453721	chr1:185081931-185081932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577004491	chr1:185081938-185081939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191759012	chr1:185081947-185081948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184012494	chr1:185081957-185081958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568359324	chr1:185081977-185081978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535074014	chr1:185081978-185081979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79954848	chr1:185081994-185081995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543054003	chr1:185082005-185082006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34916432	chr1:185082023-185082024	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs79146819	chr1:185082078-185082079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540955777	chr1:185082099-185082100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76259940	chr1:185082111-185082112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78669767	chr1:185082120-185082121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550355161	chr1:185082130-185082131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs151243855	chr1:185082155-185082156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529606755	chr1:185082165-185082166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537119439	chr1:185082186-185082187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547806762	chr1:185082194-185082195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566161273	chr1:185082199-185082200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533832564	chr1:185082206-185082207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558855612	chr1:185082207-185082208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570552237	chr1:185082214-185082215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538048639	chr1:185082227-185082228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12098126	chr1:185082264-185082265	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs375700100	chr1:185082273-185082274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575824075	chr1:185082331-185082332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140641238	chr1:185082347-185082348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371076878	chr1:185082490-185082491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373729680	chr1:185082494-185082495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188697226	chr1:185082527-185082528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113785123	chr1:185082569-185082570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115271703	chr1:185082590-185082591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540566119	chr1:185082614-185082615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565573562	chr1:185082653-185082654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540361859	chr1:185082693-185082694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs55812604	chr1:185082713-185082714	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs150060156	chr1:185082715-185082716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192218782	chr1:185082733-185082734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529722291	chr1:185082846-185082847	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs371899677	chr1:185082877-185082878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs566124625	chr1:185082890-185082891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs11801187	chr1:185082941-185082942	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs527330378	chr1:185082957-185082958	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs552140636	chr1:185082968-185082969	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs376700397	chr1:185082984-185082985	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs570735709	chr1:185083027-185083028	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs12745205	chr1:185083029-185083030	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs371056184	chr1:185083101-185083102	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs567565192	chr1:185083151-185083152	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	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
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
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	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
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Renal cell carcinoma	18765545	CNVD
Nephroblastoma	17189400	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Barrett''s syndrome	19417022	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	19197363	CNVD

Chromatin state (count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185018400-185101800	Weak transcription	Fetal Brain Male	brain
2	chr1:185054400-185101800	Weak transcription	A549	lung
3	chr1:185055400-185096200	Weak transcription	Hela-S3	cervix
4	chr1:185056200-185124200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr1:185057600-185094600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr1:185058600-185089000	Weak transcription	Ovary	ovary
7	chr1:185058800-185093600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr1:185059000-185124800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr1:185065800-185088600	Weak transcription	NHDF-Ad	bronchial
10	chr1:185067800-185095400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:185068400-185110200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr1:185069400-185091000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:185069600-185088200	Weak transcription	Fetal Lung	lung
14	chr1:185070000-185101400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr1:185070200-185088800	Weak transcription	HSMM	muscle
16	chr1:185070400-185089200	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr1:185073600-185088200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr1:185073600-185092800	Weak transcription	Fetal Kidney	kidney
19	chr1:185073600-185115000	Weak transcription	NH-A	brain
20	chr1:185073800-185088600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr1:185073800-185088600	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr1:185074000-185088600	Weak transcription	NHLF	lung
23	chr1:185077400-185088200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:185077800-185086400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:185078800-185088800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:185078800-185102000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr1:185079800-185102000	Weak transcription	Small Intestine	intestine
28	chr1:185080000-185101000	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr1:185081200-185091400	Weak transcription	GM12878-XiMat	blood
30	chr1:185081600-185091000	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr1:185081800-185088600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr1:185081800-185088800	Weak transcription	Stomach Smooth Muscle	stomach
33	chr1:185081800-185092800	Weak transcription	HUVEC	blood vessel
34	chr1:185082000-185085800	Weak transcription	Primary hematopoietic stem cells	blood
35	chr1:185082000-185086000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:185082000-185088600	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr1:185082000-185092800	Weak transcription	K562	blood
38	chr1:185082200-185088600	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr1:185082200-185095200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:185082400-185085800	Weak transcription	Primary B cells from cord blood	blood
41	chr1:185082400-185086000	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr1:185082400-185088800	Weak transcription	Brain Cingulate Gyrus	brain
43	chr1:185082400-185093600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:185082600-185086400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr1:185082600-185088200	Weak transcription	Brain Substantia Nigra	brain
46	chr1:185082600-185100400	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr1:185082600-185101400	Weak transcription	Esophagus	oesophagus
48	chr1:185082600-185125400	Weak transcription	Spleen	Spleen
49	chr1:185082800-185086400	Weak transcription	Dnd41	blood
50	chr1:185082800-185088200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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