Variant report

Variant	nsv1012919
Chromosome Location	chr1:169200982-169324750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1090)
CpG islands
(count:183)
Chromatin interactive
region (count:49)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1090 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:169209995-169210076	K562	blood:	n/a	n/a
2	ARID3A	chr1:169219638-169220576	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:169281179-169282005	K562	blood:	n/a	n/a
4	ARID3A	chr1:169296010-169296494	K562	blood:	n/a	n/a
5	ARID3A	chr1:169317650-169318046	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:169317568-169318031	K562	blood:	n/a	n/a
7	ARID3A	chr1:169278254-169279195	K562	blood:	n/a	n/a
8	ARID3A	chr1:169235297-169235803	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:169307797-169308402	K562	blood:	n/a	n/a
10	ARID3A	chr1:169240319-169240724	K562	blood:	n/a	n/a
11	ARID3A	chr1:169273481-169273723	HepG2	liver:	n/a	n/a
12	ARID3A	chr1:169256764-169256929	K562	blood:	n/a	n/a
13	ARID3A	chr1:169290801-169291112	K562	blood:	n/a	n/a
14	ATF1	chr1:169281294-169281860	K562	blood:	n/a	n/a
15	ATF1	chr1:169296174-169296480	K562	blood:	n/a	n/a
16	ATF1	chr1:169210187-169210271	K562	blood:	n/a	n/a
17	ATF1	chr1:169278356-169278862	K562	blood:	n/a	n/a
18	ATF1	chr1:169315537-169315783	K562	blood:	n/a	n/a
19	ATF1	chr1:169290858-169290985	K562	blood:	n/a	n/a
20	ATF1	chr1:169271654-169271659	K562	blood:	n/a	n/a
21	ATF1	chr1:169240334-169240757	K562	blood:	n/a	n/a
22	ATF3	chr1:169278317-169278743	K562	blood:	n/a	n/a
23	ATF3	chr1:169281286-169281872	K562	blood:	n/a	n/a
24	ATF3	chr1:169290831-169291142	K562	blood:	n/a	n/a
25	BACH1	chr1:169307787-169307975	K562	blood:	n/a	n/a
26	BACH1	chr1:169278455-169278933	K562	blood:	n/a	n/a
27	BHLHE40	chr1:169297163-169297496	K562	blood:	n/a	n/a
28	BHLHE40	chr1:169278347-169278984	K562	blood:	n/a	n/a
29	BHLHE40	chr1:169240319-169240648	K562	blood:	n/a	n/a
30	BHLHE40	chr1:169281212-169281825	K562	blood:	n/a	n/a
31	BRCA1	chr1:169281416-169281820	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr1:169290749-169291160	HCT-116	colon:	n/a	n/a
33	CBX3	chr1:169296071-169296561	K562	blood:	n/a	n/a
34	CBX3	chr1:169297109-169297443	K562	blood:	n/a	n/a
35	CBX3	chr1:169281152-169281893	HCT-116	colon:	n/a	n/a
36	CBX3	chr1:169250809-169251199	K562	blood:	n/a	n/a
37	CBX3	chr1:169310451-169310851	K562	blood:	n/a	n/a
38	CBX3	chr1:169281110-169281886	K562	blood:	n/a	n/a
39	CBX3	chr1:169278281-169279082	K562	blood:	n/a	n/a
40	CBX3	chr1:169277513-169278118	K562	blood:	n/a	n/a
41	CBX3	chr1:169298616-169298978	K562	blood:	n/a	n/a
42	CCNT2	chr1:169278275-169279107	K562	blood:	n/a	n/a
43	CCNT2	chr1:169281329-169281758	K562	blood:	n/a	n/a
44	CCNT2	chr1:169296269-169296469	K562	blood:	n/a	n/a
45	CEBPB	chr1:169290834-169291182	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr1:169281471-169281820	K562	blood:	n/a	n/a
47	CEBPB	chr1:169307502-169307646	HepG2	liver:	n/a	chr1:169307574-169307585
48	CEBPB	chr1:169290880-169291202	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr1:169290842-169291192	A549	lung:	n/a	n/a
50	CEBPB	chr1:169278235-169279153	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:169294011-169294061	AG04450	lung:	fetal
2	chr1:169294011-169294061	IMR90	lung:	fetal
3	chr1:169258066-169258116	NB4	blood:	n/a
4	chr1:169305302-169305352	AG10803	skin:	n/a
5	chr1:169258066-169258116	AoSMC	blood vessel:	n/a
6	chr1:169258066-169258116	A549	lung:	n/a
7	chr1:169305302-169305352	MCF-7	breast:	n/a
8	chr1:169258066-169258116	H1-hESC	embryonic stem cell:	embryo
9	chr1:169294011-169294061	NB4	blood:	n/a
10	chr1:169294011-169294061	U87	brain:	n/a
11	chr1:169305302-169305352	GM12891	blood:	n/a
12	chr1:169258066-169258116	MCF-7	breast:	n/a
13	chr1:169305302-169305352	GM12892	blood:	n/a
14	chr1:169305302-169305352	ProgFib	skin:	n/a
15	chr1:169258066-169258116	HRCEpiC	kidney:	n/a
16	chr1:169305302-169305352	AG09319	gingival:	n/a
17	chr1:169294011-169294061	SK-N-SH_RA	brain:	n/a
18	chr1:169258066-169258116	NT2-D1	testis:	n/a
19	chr1:169305302-169305352	LNCaP	prostate:	n/a
20	chr1:169305302-169305352	RPTEC	kidney:	n/a
21	chr1:169305302-169305352	Caco-2	colon:	n/a
22	chr1:169305302-169305352	T-47D	breast:	n/a
23	chr1:169305302-169305352	AG09309	skin:	n/a
24	chr1:169305302-169305352	ovcar-3	ovarian:	n/a
25	chr1:169258066-169258116	AG09319	gingival:	n/a
26	chr1:169294011-169294061	LNCaP	prostate:	n/a
27	chr1:169305302-169305352	NT2-D1	testis:	n/a
28	chr1:169258066-169258116	SK-N-SH	brain:	n/a
29	chr1:169294011-169294061	Caco-2	colon:	n/a
30	chr1:169305302-169305352	HUVEC	blood vessel:	n/a
31	chr1:169305302-169305352	Hepatocyte	liver:	n/a
32	chr1:169294011-169294061	ovcar-3	ovarian:	n/a
33	chr1:169305302-169305352	AG04450	lung:	fetal
34	chr1:169294011-169294061	GM12892	blood:	n/a
35	chr1:169258066-169258116	U87	brain:	n/a
36	chr1:169294011-169294061	HEK293	kidney:	embryo
37	chr1:169305302-169305352	NHBE	bronchial:	n/a
38	chr1:169305302-169305352	NB4	blood:	n/a
39	chr1:169294011-169294061	Jurkat	blood:	n/a
40	chr1:169305302-169305352	K562	blood:	n/a
41	chr1:169294011-169294061	NH-A	brain:	n/a
42	chr1:169258066-169258116	HMEC	breast:	n/a
43	chr1:169305302-169305352	HNPCEpiC	eye:	n/a
44	chr1:169258066-169258116	NH-A	brain:	n/a
45	chr1:169258066-169258116	HCF	heart:	n/a
46	chr1:169305302-169305352	GM12878	blood:	n/a
47	chr1:169294011-169294061	HRPEpiC	eye:	n/a
48	chr1:169305302-169305352	CMK	blood:	n/a
49	chr1:169258066-169258116	GM06990	blood:	n/a
50	chr1:169294011-169294061	HL-60	blood:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:169315565..169317290-chr1:169336784..169338618,2	MCF-7	breast:
2	chr1:151495856..151496660-chr1:169285854..169286373,2	MCF-7	breast:
3	chr1:169201903..169204438-chr1:169206741..169208381,2	MCF-7	breast:
4	chr1:169275275..169277238-chr1:169338409..169341241,2	K562	blood:
5	chr1:169075421..169077464-chr1:169318812..169321562,2	MCF-7	breast:
6	chr1:169280326..169283147-chr1:169287038..169289000,3	K562	blood:
7	chr1:168605132..168606019-chr1:169317390..169318347,3	MCF-7	breast:
8	chr1:169210215..169210976-chr2:173891921..173892590,2	MCF-7	breast:
9	chr1:169284485..169288949-chr1:169289510..169292758,5	K562	blood:
10	chr1:169079372..169082049-chr1:169315164..169316948,2	MCF-7	breast:
11	chr1:169073990..169076920-chr1:169277266..169279793,2	K562	blood:
12	chr1:169074524..169076141-chr1:169277418..169279105,2	MCF-7	breast:
13	chr1:169265989..169270734-chr1:169271559..169276402,6	K562	blood:
14	chr1:169249538..169251657-chr1:169297595..169299857,2	MCF-7	breast:
15	chr1:169277364..169279006-chr1:169286069..169288203,2	K562	blood:
16	chr1:168572452..168573406-chr1:169319144..169320245,3	MCF-7	breast:
17	chr1:169285804..169288205-chr1:169289257..169290945,2	MCF-7	breast:
18	chr1:169284485..169288949-chr1:169289510..169292758,5	K562	blood:
19	chr1:169315275..169317459-chr1:169319904..169321487,2	K562	blood:
20	chr1:169266400..169268623-chr1:169277324..169279302,2	K562	blood:
21	chr1:169291437..169294345-chr1:169295475..169297579,2	K562	blood:
22	chr1:169208518..169210284-chr1:169213594..169216583,2	K562	blood:
23	chr1:169210444..169212042-chr1:169215118..169217438,2	K562	blood:
24	chr1:169210444..169212042-chr1:169215118..169217438,2	K562	blood:
25	chr1:169317063..169319375-chr1:169454243..169457078,2	K562	blood:
26	chr1:168604062..168606034-chr1:169316647..169318325,2	MCF-7	breast:
27	chr1:169277364..169279006-chr1:169286069..169288203,2	K562	blood:
28	chr1:168605217..168605845-chr1:169317745..169318328,2	MCF-7	breast:
29	chr1:169276344..169278316-chr1:169279851..169282220,2	MCF-7	breast:
30	chr1:169267146..169270567-chr1:169272063..169277859,6	K562	blood:
31	chr1:169281102..169283906-chr1:169293701..169295205,2	K562	blood:
32	chr1:169266400..169268623-chr1:169277324..169279302,2	K562	blood:
33	chr1:168606300..168607332-chr1:169317339..169318501,5	MCF-7	breast:
34	chr1:168572459..168573424-chr1:169317442..169318283,3	MCF-7	breast:
35	chr1:169279086..169281627-chr1:169295579..169298053,2	K562	blood:
36	chr1:169315069..169315689-chr12:40537506..40538182,2	MCF-7	breast:
37	chr1:168572446..168573392-chr1:169317346..169318310,9	MCF-7	breast:
38	chr1:169276766..169278589-chr1:169293120..169295874,2	K562	blood:
39	chr1:169208518..169210284-chr1:169213594..169216583,2	K562	blood:
40	chr1:168606588..168607302-chr1:169317375..169317960,4	K562	blood:
41	chr1:169201903..169204438-chr1:169206741..169208381,2	MCF-7	breast:
42	chr1:169285804..169288205-chr1:169289257..169290945,2	MCF-7	breast:
43	chr1:169315275..169317459-chr1:169319904..169321487,2	K562	blood:
44	chr1:168572454..168573380-chr1:169317397..169317940,2	K562	blood:
45	chr1:169192162..169194718-chr1:169212473..169215131,2	K562	blood:
46	chr1:169249538..169251657-chr1:169297595..169299857,2	MCF-7	breast:
47	chr1:169281102..169283906-chr1:169293701..169295205,2	K562	blood:
48	chr1:169074233..169076975-chr1:169305582..169307611,2	K562	blood:
49	chr1:169280326..169283147-chr1:169287038..169289000,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BLZF1-1	chr1:169279903-169280009	ENSG00000235575.1
2	lnc-BLZF1-1	chr1:169291457-169291717	ENSG00000235575.1

No data

Variant related genes	Relation type
NME7	TF binding region
ENSG00000235575	TF binding region
NME7	CpG island
ENSG00000235575	CpG island
ENSG00000117475	chromatin interactions
ENSG00000213062	chromatin interactions
ENSG00000143156	chromatin interactions
ENSG00000235575	chromatin interactions
ENSG00000143153	chromatin interactions
ENSG00000117479	chromatin interactions

Extended variants
information (count: 4547 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4547 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190736115	chr1:169200995-169200996	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183246163	chr1:169200999-169201000	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543526328	chr1:169201001-169201002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186565780	chr1:169201021-169201022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146331441	chr1:169201027-169201028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541589819	chr1:169201074-169201075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77271624	chr1:169201091-169201092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116142818	chr1:169201097-169201098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369968661	chr1:169201110-169201111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548317205	chr1:169201149-169201150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs36013240	chr1:169201157-169201158	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs530947843	chr1:169201183-169201184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552245148	chr1:169201228-169201229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189777825	chr1:169201283-169201284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538451164	chr1:169201344-169201345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572045953	chr1:169201361-169201362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553896581	chr1:169201370-169201371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115370596	chr1:169201386-169201387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564607977	chr1:169201403-169201404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs578057396	chr1:169201428-169201429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542337781	chr1:169201450-169201451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543863575	chr1:169201470-169201471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536524343	chr1:169201561-169201562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2157597	chr1:169201567-169201568	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs114426084	chr1:169201579-169201580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200829426	chr1:169201603-169201604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75903162	chr1:169201606-169201607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2901031	chr1:169201607-169201608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543587149	chr1:169201656-169201657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10753785	chr1:169201728-169201729	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs201867013	chr1:169201738-169201739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376324490	chr1:169201746-169201747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541283015	chr1:169201761-169201762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544707263	chr1:169201762-169201763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114054371	chr1:169201788-169201789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182882268	chr1:169201789-169201790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs111237631	chr1:169201795-169201796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12401966	chr1:169201797-169201798	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs530813236	chr1:169201802-169201803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200223276	chr1:169201803-169201804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200074206	chr1:169201804-169201805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570621572	chr1:169201829-169201830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528536506	chr1:169201841-169201842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12118533	chr1:169201845-169201846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35320726	chr1:169201864-169201865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370721085	chr1:169201930-169201931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12126266	chr1:169201933-169201934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs536192785	chr1:169202092-169202093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376962870	chr1:169202115-169202116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554842777	chr1:169202116-169202117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	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
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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:988 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169172400-169207600	Weak transcription	Esophagus	oesophagus
2	chr1:169172600-169227000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:169173200-169202000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr1:169176600-169206200	Weak transcription	Aorta	Aorta
5	chr1:169177400-169207400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr1:169180000-169210000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:169180600-169206200	Weak transcription	Left Ventricle	heart
8	chr1:169182000-169201000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr1:169182800-169205400	Weak transcription	Adipose Nuclei	Adipose
10	chr1:169184400-169206200	Weak transcription	Lung	lung
11	chr1:169184800-169207400	Weak transcription	Ovary	ovary
12	chr1:169187600-169207800	Weak transcription	Primary T cells from cord blood	blood
13	chr1:169187800-169211800	Weak transcription	Primary hematopoietic stem cells	blood
14	chr1:169192200-169209600	Weak transcription	NHEK	skin
15	chr1:169192400-169210000	Weak transcription	Brain Hippocampus Middle	brain
16	chr1:169192600-169202800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr1:169194000-169210000	Weak transcription	NHDF-Ad	bronchial
18	chr1:169194800-169207400	Weak transcription	Primary B cells from cord blood	blood
19	chr1:169194800-169214000	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr1:169195200-169207600	Weak transcription	Fetal Lung	lung
21	chr1:169195400-169207600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:169197000-169204600	Weak transcription	HUVEC	blood vessel
23	chr1:169197200-169206200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:169197200-169207600	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr1:169197200-169210200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr1:169197600-169210200	Weak transcription	Brain Substantia Nigra	brain
27	chr1:169197800-169202200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr1:169198000-169209800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:169198600-169205200	Weak transcription	Fetal Kidney	kidney
30	chr1:169199200-169205000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr1:169199200-169210200	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr1:169199200-169211600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr1:169199600-169209800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:169200600-169201000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:169200600-169201200	Enhancers	Colon Smooth Muscle	Colon
36	chr1:169200600-169201200	Enhancers	Rectal Smooth Muscle	rectum
37	chr1:169200800-169201000	Enhancers	Psoas Muscle	Psoas
38	chr1:169200800-169204000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr1:169201000-169207800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr1:169201000-169212800	Weak transcription	Psoas Muscle	Psoas
41	chr1:169201200-169204600	Weak transcription	Rectal Smooth Muscle	rectum
42	chr1:169201200-169205000	Weak transcription	Colon Smooth Muscle	Colon
43	chr1:169202400-169208800	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr1:169202800-169203200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:169202800-169205400	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr1:169203200-169205400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:169203600-169206800	Enhancers	Liver	Liver
48	chr1:169204000-169204200	Enhancers	HepG2	liver
49	chr1:169204600-169205000	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr1:169204600-169205200	Enhancers	HUVEC	blood vessel

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