Variant report

Variant	nsv1005067
Chromosome Location	chr1:246289451-246619260
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3495)
CpG islands
(count:2257)
Chromatin interactive
region (count:215)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3495 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246329377-246329956	K562	blood:	n/a	n/a
2	ARID3A	chr1:246383173-246383457	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:246468839-246469426	K562	blood:	n/a	n/a
4	ARID3A	chr1:246614088-246614383	HepG2	liver:	n/a	chr1:246614110-246614126
5	ARID3A	chr1:246587912-246588291	K562	blood:	n/a	n/a
6	ARID3A	chr1:246472537-246472962	K562	blood:	n/a	n/a
7	ARID3A	chr1:246315871-246317843	K562	blood:	n/a	n/a
8	ARID3A	chr1:246443886-246444158	K562	blood:	n/a	n/a
9	ARID3A	chr1:246409804-246409947	K562	blood:	n/a	n/a
10	ARID3A	chr1:246339570-246339954	K562	blood:	n/a	n/a
11	ARID3A	chr1:246378433-246378571	HepG2	liver:	n/a	n/a
12	ARID3A	chr1:246476713-246476913	K562	blood:	n/a	n/a
13	ARID3A	chr1:246303013-246303421	K562	blood:	n/a	n/a
14	ARID3A	chr1:246305649-246306059	K562	blood:	n/a	n/a
15	ARID3A	chr1:246351173-246351659	K562	blood:	n/a	n/a
16	ARID3A	chr1:246345414-246346141	K562	blood:	n/a	n/a
17	ARID3A	chr1:246317239-246317589	HepG2	liver:	n/a	n/a
18	ARID3A	chr1:246332132-246332717	K562	blood:	n/a	n/a
19	ARID3A	chr1:246514223-246514241	K562	blood:	n/a	n/a
20	ARID3A	chr1:246364034-246364381	K562	blood:	n/a	n/a
21	ARID3A	chr1:246495436-246495765	K562	blood:	n/a	n/a
22	ARID3A	chr1:246614048-246614417	K562	blood:	n/a	chr1:246614110-246614126
23	ARID3A	chr1:246536567-246536576	K562	blood:	n/a	n/a
24	ARID3A	chr1:246591789-246592119	K562	blood:	n/a	n/a
25	ARID3A	chr1:246340416-246340426	K562	blood:	n/a	n/a
26	ARID3A	chr1:246303129-246303329	HepG2	liver:	n/a	n/a
27	ARID3A	chr1:246378134-246379212	K562	blood:	n/a	n/a
28	ARID3A	chr1:246306858-246307142	K562	blood:	n/a	n/a
29	ARID3A	chr1:246469874-246470465	K562	blood:	n/a	n/a
30	ARID3A	chr1:246351102-246351709	HepG2	liver:	n/a	n/a
31	ARID3A	chr1:246333485-246334689	K562	blood:	n/a	n/a
32	ARID3A	chr1:246444896-246445377	HepG2	liver:	n/a	n/a
33	ARID3A	chr1:246297019-246297023	K562	blood:	n/a	n/a
34	ARID3A	chr1:246339492-246340117	HepG2	liver:	n/a	n/a
35	ATF1	chr1:246469981-246470295	K562	blood:	n/a	n/a
36	ATF1	chr1:246332388-246332644	K562	blood:	n/a	n/a
37	ATF1	chr1:246376288-246376805	K562	blood:	n/a	n/a
38	ATF1	chr1:246317155-246317561	K562	blood:	n/a	n/a
39	ATF1	chr1:246588435-246588914	K562	blood:	n/a	n/a
40	ATF1	chr1:246304350-246304649	K562	blood:	n/a	n/a
41	ATF1	chr1:246591887-246592268	K562	blood:	n/a	n/a
42	ATF1	chr1:246363474-246363487	K562	blood:	n/a	n/a
43	ATF1	chr1:246589653-246589853	K562	blood:	n/a	n/a
44	ATF1	chr1:246305671-246306307	K562	blood:	n/a	n/a
45	ATF1	chr1:246303038-246303366	K562	blood:	n/a	n/a
46	ATF1	chr1:246445017-246445192	K562	blood:	n/a	n/a
47	ATF1	chr1:246378205-246378667	K562	blood:	n/a	n/a
48	ATF1	chr1:246495450-246495686	K562	blood:	n/a	n/a
49	ATF1	chr1:246316226-246316752	K562	blood:	n/a	n/a
50	ATF1	chr1:246329490-246330061	K562	blood:	n/a	n/a

(count:2257 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246518620-246518670	HMEC	breast:	n/a
2	chr1:246582116-246582166	NHBE	bronchial:	n/a
3	chr1:246310411-246310461	AG09319	gingival:	n/a
4	chr1:246315928-246315978	AG04449	skin:	fetal
5	chr1:246415568-246415618	PFSK-1	brain:	n/a
6	chr1:246415568-246415618	HCF	heart:	n/a
7	chr1:246414840-246414890	HCM	heart:	n/a
8	chr1:246429789-246429839	IMR90	lung:	fetal
9	chr1:246446300-246446350	SK-N-MC	brain:	n/a
10	chr1:246581705-246581755	NT2-D1	testis:	n/a
11	chr1:246324811-246324861	AG09309	skin:	n/a
12	chr1:246324811-246324861	HRPEpiC	eye:	n/a
13	chr1:246315928-246315978	AG09319	gingival:	n/a
14	chr1:246363574-246363624	BJ	skin:	n/a
15	chr1:246518620-246518670	HCT-116	colon:	n/a
16	chr1:246310485-246310535	NHDF-neo	bronchial:	n/a
17	chr1:246310349-246310399	GM12891	blood:	n/a
18	chr1:246415568-246415618	HepG2	liver:	n/a
19	chr1:246304208-246304258	SK-N-SH	brain:	n/a
20	chr1:246414665-246414715	HRCEpiC	kidney:	n/a
21	chr1:246305399-246305449	NHDF-neo	bronchial:	n/a
22	chr1:246378510-246378560	SAEC	small airway:	n/a
23	chr1:246370933-246370983	NB4	blood:	n/a
24	chr1:246320475-246320525	NT2-D1	testis:	n/a
25	chr1:246599230-246599280	HCPEpiC	choroid plexus:	n/a
26	chr1:246416688-246416738	HNPCEpiC	eye:	n/a
27	chr1:246582071-246582121	GM06990	blood:	n/a
28	chr1:246363574-246363624	GM19239	blood:	n/a
29	chr1:246592123-246592173	PFSK-1	brain:	n/a
30	chr1:246304208-246304258	PrEC	prostate:	n/a
31	chr1:246518671-246518721	LNCaP	prostate:	n/a
32	chr1:246451744-246451794	HepG2	liver:	n/a
33	chr1:246363574-246363624	AoSMC	blood vessel:	n/a
34	chr1:246304208-246304258	GM12878	blood:	n/a
35	chr1:246415568-246415618	HMEC	breast:	n/a
36	chr1:246415568-246415618	SKMC	muscle:	n/a
37	chr1:246383021-246383071	NHDF-neo	bronchial:	n/a
38	chr1:246320475-246320525	K562	blood:	n/a
39	chr1:246582116-246582166	HIPEpiC	eye:	n/a
40	chr1:246415165-246415215	ProgFib	skin:	n/a
41	chr1:246370933-246370983	U87	brain:	n/a
42	chr1:246414840-246414890	HMEC	breast:	n/a
43	chr1:246305399-246305449	HCT-116	colon:	n/a
44	chr1:246310349-246310399	ovcar-3	ovarian:	n/a
45	chr1:246363697-246363747	PANC-1	pancreas:	n/a
46	chr1:246324811-246324861	Jurkat	blood:	n/a
47	chr1:246415214-246415264	HCM	heart:	n/a
48	chr1:246582071-246582121	HRE	kidney:	n/a
49	chr1:246613311-246613361	SK-N-SH	brain:	n/a
50	chr1:246518620-246518670	HCF	heart:	n/a

(count:215 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
2	chr1:246349919..246351757-chr1:246469177..246472168,2	K562	blood:
3	chr1:246377128..246379304-chr1:246383039..246386771,4	K562	blood:
4	chr1:246304167..246305874-chr1:246388175..246390883,2	K562	blood:
5	chr1:246356282..246358197-chr1:246359640..246362588,2	K562	blood:
6	chr1:246339516..246341539-chr1:246347667..246350231,2	K562	blood:
7	chr1:246331255..246333673-chr1:246367321..246369174,2	K562	blood:
8	chr1:246331480..246334124-chr1:246374874..246378179,3	K562	blood:
9	chr1:246280977..246283583-chr1:246293075..246294751,2	K562	blood:
10	chr1:246339928..246341615-chr1:246379189..246380773,2	K562	blood:
11	chr1:246175270..246176065-chr1:246443608..246444506,2	MCF-7	breast:
12	chr1:246283420..246285442-chr1:246309239..246311230,2	K562	blood:
13	chr1:246303495..246306229-chr1:246309475..246311302,2	MCF-7	breast:
14	chr1:246330748..246332762-chr1:246362456..246364545,2	K562	blood:
15	chr1:246295456..246296994-chr1:246303887..246305807,2	K562	blood:
16	chr1:246286174..246287745-chr1:246302664..246304849,2	K562	blood:
17	chr1:246303120..246308295-chr1:246314639..246320743,10	K562	blood:
18	chr1:246175508..246176198-chr1:246613763..246614605,2	K562	blood:
19	chr1:246471340..246473899-chr1:246474297..246475919,2	K562	blood:
20	chr1:246280572..246283583-chr1:246290379..246294751,4	K562	blood:
21	chr1:246594102..246596959-chr1:246598193..246600594,2	K562	blood:
22	chr1:246374232..246375756-chr1:246376592..246378165,2	K562	blood:
23	chr1:246297174..246299753-chr1:246320284..246323072,2	K562	blood:
24	chr1:246363848..246365407-chr1:246365927..246368390,2	K562	blood:
25	chr1:246289069..246291889-chr1:246319993..246322054,2	K562	blood:
26	chr1:246353361..246355066-chr1:246367112..246369364,2	K562	blood:
27	chr1:246151420..246154131-chr1:246468233..246469966,2	K562	blood:
28	chr1:246497788..246499304-chr1:246499416..246501844,2	MCF-7	breast:
29	chr1:246323883..246327083-chr1:246329402..246331782,5	K562	blood:
30	chr1:246458189..246460474-chr1:246462017..246465759,3	K562	blood:
31	chr1:246303120..246308295-chr1:246314639..246320743,10	K562	blood:
32	chr1:246297174..246299753-chr1:246320284..246323072,2	K562	blood:
33	chr1:246361048..246363741-chr1:246366833..246369637,3	K562	blood:
34	chr1:246392871..246395828-chr1:246399439..246401491,2	K562	blood:
35	chr1:246389393..246391368-chr1:246392967..246394891,2	K562	blood:
36	chr1:246482242..246483844-chr1:246486769..246488361,2	MCF-7	breast:
37	chr1:246452108..246454615-chr1:246458116..246460010,2	K562	blood:
38	chr1:246323812..246327417-chr1:246344916..246347036,3	K562	blood:
39	chr1:246280440..246281134-chr1:246613800..246614445,2	MCF-7	breast:
40	chr1:246346688..246348274-chr1:246353285..246354827,2	K562	blood:
41	chr1:246587797..246590207-chr1:246590613..246593809,3	K562	blood:
42	chr1:246278749..246281660-chr1:246307722..246309243,2	K562	blood:
43	chr1:246303201..246305225-chr1:246319673..246321317,2	MCF-7	breast:
44	chr1:246175245..246176233-chr1:246613342..246615151,4	MCF-7	breast:
45	chr1:246057307..246059352-chr1:246513090..246515764,2	K562	blood:
46	chr1:246471340..246473899-chr1:246474297..246475919,2	K562	blood:
47	chr1:246314921..246318931-chr1:246320889..246326868,8	K562	blood:
48	chr1:246287445..246289501-chr1:246320750..246323566,2	MCF-7	breast:
49	chr1:246383754..246387049-chr1:246387673..246391431,4	K562	blood:
50	chr1:246175301..246176197-chr1:246366037..246366781,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNST-4	chr1:246342080-246342506	NONHSAT010702
2	lnc-TFB2M-2	chr1:246484965-246485170	ENSG00000230184.1
3	lnc-TFB2M-2	chr1:246485586-246485740	ENSG00000230184.1

No data

Variant related genes	Relation type
CHCHD4P5	TF binding region
SMYD3	TF binding region
SMYD3-IT1	TF binding region
RNU6-1283P	TF binding region
ENSG00000207326	TF binding region
CHCHD4P5	CpG island
SMYD3	CpG island
SMYD3-IT1	CpG island
RNU6-1283P	CpG island
ENSG00000207326	CpG island
ENSG00000202184	chromatin interactions
ENSG00000230184	chromatin interactions
ENSG00000185420	chromatin interactions
ENSG00000207326	chromatin interactions

Extended variants
information (count: 13485 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:13485 , 50 per page) page: 1 2 3 4 5 6 7 ... 270

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149357553	chr1:246289559-246289560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189119327	chr1:246289560-246289561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144662188	chr1:246289578-246289579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181060246	chr1:246289582-246289583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112375247	chr1:246289603-246289604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575491541	chr1:246289643-246289644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187182105	chr1:246289653-246289654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560056422	chr1:246289658-246289659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554295758	chr1:246289662-246289663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2066029	chr1:246289665-246289666	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs1547743	chr1:246289675-246289676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4528086	chr1:246289691-246289692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540345530	chr1:246289734-246289735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6656104	chr1:246289752-246289753	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs75845327	chr1:246289816-246289817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs72772566	chr1:246289848-246289849	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs4654209	chr1:246289853-246289854	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs531139601	chr1:246289867-246289868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs367823116	chr1:246289900-246289901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551241861	chr1:246289920-246289921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567341269	chr1:246289954-246289955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141976202	chr1:246289997-246289998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111279290	chr1:246290062-246290063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75641185	chr1:246290085-246290086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4654210	chr1:246290120-246290121	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs566587318	chr1:246290145-246290146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538739375	chr1:246290161-246290162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558518592	chr1:246290232-246290233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569011056	chr1:246290263-246290264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367872722	chr1:246290289-246290290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4654211	chr1:246290291-246290292	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs554814045	chr1:246290344-246290345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574507307	chr1:246290375-246290376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376364475	chr1:246290400-246290401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374809623	chr1:246290480-246290481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6659308	chr1:246290486-246290487	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs553911665	chr1:246290514-246290515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146124693	chr1:246290522-246290523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190914788	chr1:246290530-246290531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559830978	chr1:246290567-246290568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140155554	chr1:246290584-246290585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114020544	chr1:246290607-246290608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561200412	chr1:246290683-246290684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114634706	chr1:246290758-246290759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143790834	chr1:246290880-246290881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78604191	chr1:246290907-246290908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532525009	chr1:246290936-246290937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111937620	chr1:246290955-246290956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146224576	chr1:246290957-246290958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538017350	chr1:246290973-246290974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Schizophrenia	20967226	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD

Chromatin state (count:2215 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246271200-246302200	Weak transcription	Osteobl	bone
2	chr1:246272400-246312000	Weak transcription	Gastric	stomach
3	chr1:246274000-246301400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:246277400-246297200	Weak transcription	Aorta	Aorta
5	chr1:246277800-246327800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:246280600-246294200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr1:246281000-246304000	Weak transcription	Primary T cells from cord blood	blood
8	chr1:246281200-246310800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:246281200-246311400	Weak transcription	Primary B cells from cord blood	blood
10	chr1:246281200-246311400	Weak transcription	Primary hematopoietic stem cells	blood
11	chr1:246281800-246306400	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr1:246284600-246291400	Weak transcription	K562	blood
13	chr1:246285800-246302200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:246291400-246292200	Strong transcription	K562	blood
15	chr1:246292200-246294200	Weak transcription	K562	blood
16	chr1:246292800-246293200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:246292800-246293600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:246294000-246295000	Enhancers	HUVEC	blood vessel
19	chr1:246294200-246294600	Enhancers	Stomach Mucosa	stomach
20	chr1:246294200-246294800	Enhancers	K562	blood
21	chr1:246294800-246303000	Weak transcription	K562	blood
22	chr1:246295600-246298600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:246297200-246297400	Enhancers	Aorta	Aorta
24	chr1:246298600-246299000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:246299000-246302000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:246300600-246300800	Enhancers	A549	lung
27	chr1:246301000-246302200	Weak transcription	A549	lung
28	chr1:246301400-246301600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr1:246301400-246302600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:246301400-246303000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr1:246301400-246306600	Enhancers	NHLF	lung
32	chr1:246301600-246306600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:246302000-246303000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr1:246302000-246306600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:246302000-246306600	Enhancers	HMEC	breast
36	chr1:246302200-246302400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr1:246302200-246302400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr1:246302200-246302800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr1:246302200-246304000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:246302200-246304000	Enhancers	Placenta Amnion	Placenta Amnion
41	chr1:246302200-246304000	Enhancers	HSMM	muscle
42	chr1:246302200-246306000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr1:246302200-246306200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr1:246302200-246306400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr1:246302200-246306400	Enhancers	NHEK	skin
46	chr1:246302200-246306600	Enhancers	A549	lung
47	chr1:246302200-246306600	Enhancers	NH-A	brain
48	chr1:246302200-246306600	Enhancers	NHDF-Ad	bronchial
49	chr1:246302200-246306600	Enhancers	Osteobl	bone
50	chr1:246302400-246302600	Enhancers	Placenta	Placenta

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