Variant report

Variant	nsv872178
Chromosome Location	chr1:120111002-120150452
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:120125462-120125747	K562	blood:	n/a	n/a
2	BRCA1	chr1:120125543-120125709	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr1:120144741-120145077	HepG2	liver:	n/a	chr1:120144889-120144900
4	CEBPB	chr1:120144827-120145081	Hela-S3	cervix:	n/a	chr1:120144889-120144900
5	CEBPB	chr1:120112658-120112932	K562	blood:	n/a	chr1:120112801-120112814
6	CEBPB	chr1:120144744-120145076	A549	lung:	n/a	chr1:120144889-120144900
7	CEBPB	chr1:120142586-120142702	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:120112719-120112961	K562	blood:	n/a	chr1:120112801-120112814
9	CEBPB	chr1:120123093-120123321	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr1:120144888-120144965	H1-hESC	embryonic stem cell:	n/a	chr1:120144889-120144900
11	CTCF	chr1:120150126-120150347	A549	lung:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
12	CTCF	chr1:120112982-120113171	Kidney_OC	kidney:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
13	CTCF	chr1:120150135-120150298	A549	lung:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
14	CTCF	chr1:120150188-120150201	K562	blood:	n/a	n/a
15	CTCF	chr1:120125474-120125833	H1-hESC	embryonic stem cell:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
16	CTCF	chr1:120125520-120125670	NHEK	skin:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
17	CTCF	chr1:120125476-120125869	MCF-7	breast:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
18	CTCF	chr1:120125500-120125730	K562	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
19	CTCF	chr1:120125600-120125750	GM12873	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
20	CTCF	chr1:120125560-120125710	NHLF	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
21	CTCF	chr1:120150086-120150262	H1-hESC	embryonic stem cell:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
22	CTCF	chr1:120150144-120150370	GM13977	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
23	CTCF	chr1:120125433-120125813	K562	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
24	CTCF	chr1:120125580-120125730	MCF-7	breast:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
25	CTCF	chr1:120125580-120125730	HAc	cerebellar:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
26	CTCF	chr1:120128467-120128522	GM13976	blood:	n/a	n/a
27	CTCF	chr1:120125560-120125710	HRPEpiC	eye:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
28	CTCF	chr1:120112900-120113050	GM12878	blood:	n/a	n/a
29	CTCF	chr1:120150040-120150190	HAc	cerebellar:	n/a	n/a
30	CTCF	chr1:120125560-120125710	GM12873	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
31	CTCF	chr1:120125540-120125690	SK-N-SH_RA	brain:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
32	CTCF	chr1:120112935-120113098	H1-hESC	embryonic stem cell:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094
33	CTCF	chr1:120125370-120125795	H1-hESC	embryonic stem cell:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
34	CTCF	chr1:120112880-120113030	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr1:120125541-120125710	GM19239	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
36	CTCF	chr1:120125540-120125690	GM12875	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
37	CTCF	chr1:120150100-120150537	K562	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
38	CTCF	chr1:120125560-120125710	Hela-S3	cervix:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
39	CTCF	chr1:120125580-120125730	BE2_C	brain:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
40	CTCF	chr1:120125560-120125710	HMEC	breast:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
41	CTCF	chr1:120112965-120113174	LNCaP	prostate:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
42	CTCF	chr1:120125535-120125679	GM13977	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
43	CTCF	chr1:120112880-120113030	GM12870	blood:	n/a	n/a
44	CTCF	chr1:120125560-120125710	HCM	heart:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
45	CTCF	chr1:120125580-120125730	Hela-S3	cervix:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
46	CTCF	chr1:120112920-120113070	HVMF	connective:	n/a	n/a
47	CTCF	chr1:120112900-120113050	GM12866	blood:	n/a	n/a
48	CTCF	chr1:120112920-120113070	NB4	blood:	n/a	n/a
49	CTCF	chr1:120125600-120125750	GM12866	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
50	CTCF	chr1:120125540-120125690	WI-38	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120143242-120143292	PFSK-1	brain:	n/a
2	chr1:120143242-120143292	HEK293	kidney:	embryo
3	chr1:120143242-120143292	NB4	blood:	n/a
4	chr1:120143242-120143292	BE2_C	brain:	n/a
5	chr1:120143242-120143292	HepG2	liver:	n/a
6	chr1:120143242-120143292	HCT-116	colon:	n/a
7	chr1:120143242-120143292	GM06990	blood:	n/a
8	chr1:120143242-120143292	Caco-2	colon:	n/a
9	chr1:120143242-120143292	HEEpiC	esophagus:	n/a
10	chr1:120143242-120143292	HCF	heart:	n/a
11	chr1:120143242-120143292	HCM	heart:	n/a
12	chr1:120143242-120143292	NH-A	brain:	n/a
13	chr1:120143242-120143292	NHDF-neo	bronchial:	n/a
14	chr1:120143242-120143292	T-47D	breast:	n/a
15	chr1:120143242-120143292	ECC-1	luminal epithelium:	n/a
16	chr1:120143242-120143292	HUVEC	blood vessel:	n/a
17	chr1:120143242-120143292	ovcar-3	ovarian:	n/a
18	chr1:120143242-120143292	NT2-D1	testis:	n/a
19	chr1:120143242-120143292	AG09319	gingival:	n/a
20	chr1:120143242-120143292	Jurkat	blood:	n/a
21	chr1:120143242-120143292	AG09309	skin:	n/a
22	chr1:120143242-120143292	HRCEpiC	kidney:	n/a
23	chr1:120143242-120143292	HL-60	blood:	n/a
24	chr1:120143242-120143292	A549	lung:	n/a
25	chr1:120143242-120143292	LNCaP	prostate:	n/a
26	chr1:120143242-120143292	GM12892	blood:	n/a
27	chr1:120143242-120143292	HRPEpiC	eye:	n/a
28	chr1:120143242-120143292	NHBE	bronchial:	n/a
29	chr1:120143242-120143292	SK-N-SH	brain:	n/a
30	chr1:120143242-120143292	SAEC	small airway:	n/a
31	chr1:120143242-120143292	HAEpiC	amniotic membrane:	n/a
32	chr1:120143242-120143292	Hepatocyte	liver:	n/a
33	chr1:120143242-120143292	PANC-1	pancreas:	n/a
34	chr1:120143242-120143292	CMK	blood:	n/a
35	chr1:120143242-120143292	IMR90	lung:	fetal
36	chr1:120143242-120143292	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:120143242-120143292	Hela-S3	cervix:	n/a
38	chr1:120143242-120143292	HIPEpiC	eye:	n/a
39	chr1:120143242-120143292	GM12891	blood:	n/a
40	chr1:120143242-120143292	MCF10A-Er-Src	breast:	n/a
41	chr1:120143242-120143292	HMEC	breast:	n/a
42	chr1:120143242-120143292	SK-N-MC	brain:	n/a
43	chr1:120143242-120143292	GM19239	blood:	n/a
44	chr1:120143242-120143292	AoSMC	blood vessel:	n/a
45	chr1:120143242-120143292	U87	brain:	n/a
46	chr1:120143242-120143292	PrEC	prostate:	n/a
47	chr1:120143242-120143292	RPTEC	kidney:	n/a
48	chr1:120143242-120143292	H1-hESC	embryonic stem cell:	embryo
49	chr1:120143242-120143292	AG10803	skin:	n/a
50	chr1:120143242-120143292	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:120125219..120126121-chr1:120153919..120154547,2	MCF-7	breast:
2	chr1:120145059..120147660-chr1:120162749..120165475,2	MCF-7	breast:
3	chr1:120091982..120092921-chr1:120150180..120150935,3	MCF-7	breast:
4	chr1:120125200..120126107-chr1:120217588..120218409,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF697-1	chr1:120140325-120141894	ENSG00000260941.1
2	lnc-ZNF697-3	chr1:120111655-120111668	NONHSAT005569
3	lnc-PHGDH-1	chr1:120143780-120144107	ENSG00000242959.1
4	lnc-PHGDH-1	chr1:120144910-120145118	ENSG00000242959.1
5	lnc-ZNF697-3	chr1:120148999-120149695	NONHSAT005569
6	lnc-ZNF697-1	chr1:120140325-120141914	NONHSAT005570

Variant related genes	Relation type
HSD3BP4	TF binding region
LINC00622	TF binding region
GAPDHP33	TF binding region
HSD3BP5	TF binding region
HSD3BP4	CpG island
LINC00622	CpG island
GAPDHP33	CpG island
HSD3BP5	CpG island

Extended variants
information (count: 1730 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1730 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10802113	chr1:120111002-120111003	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368503144	chr1:120111034-120111035	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs587730777	chr1:120111082-120111083	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs587709898	chr1:120111096-120111097	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs188023599	chr1:120111107-120111108	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs587666365	chr1:120111134-120111135	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs193019449	chr1:120111161-120111162	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs587621193	chr1:120111191-120111192	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs587669931	chr1:120111196-120111197	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs113263264	chr1:120111200-120111201	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs371590874	chr1:120111211-120111212	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs374275870	chr1:120111214-120111215	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs368385272	chr1:120111219-120111220	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs12032931	chr1:120111235-120111236	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs587742947	chr1:120111242-120111243	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs587616338	chr1:120111243-120111244	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs12030462	chr1:120111257-120111258	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs6672394	chr1:120111261-120111262	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs148978531	chr1:120111280-120111281	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs587674728	chr1:120111332-120111333	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs587761594	chr1:120111339-120111340	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs35353663	chr1:120111368-120111369	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs587609926	chr1:120111376-120111377	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs4659206	chr1:120111383-120111384	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs587775750	chr1:120111384-120111385	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs143096679	chr1:120111397-120111398	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs146688162	chr1:120111398-120111399	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs140274289	chr1:120111431-120111432	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs587652636	chr1:120111450-120111451	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs587705865	chr1:120111460-120111461	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs587610460	chr1:120111467-120111468	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs4659207	chr1:120111468-120111469	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs117237385	chr1:120111470-120111471	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs587599914	chr1:120111542-120111543	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs587675371	chr1:120111565-120111566	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs587728589	chr1:120111569-120111570	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs145260770	chr1:120111574-120111575	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs55642553	chr1:120111598-120111599	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs55755547	chr1:120111599-120111600	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs117595240	chr1:120111631-120111632	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs137861640	chr1:120111645-120111646	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs587734279	chr1:120111646-120111647	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs587634038	chr1:120111656-120111657	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
44	rs587711061	chr1:120111657-120111658	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
45	rs386635119	chr1:120111662-120111663	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
46	rs587639738	chr1:120111663-120111664	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs587719429	chr1:120111672-120111673	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs406737	chr1:120111673-120111674	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs118009773	chr1:120111677-120111678	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs397832225	chr1:120111679-120111680	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Cancer	21272361	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120092800-120116600	Weak transcription	Spleen	Spleen
2	chr1:120106800-120111600	Weak transcription	Lung	lung
3	chr1:120106800-120112400	Enhancers	Placenta	Placenta
4	chr1:120107600-120111400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr1:120107800-120111200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr1:120107800-120111600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr1:120108000-120111200	Weak transcription	Fetal Lung	lung
8	chr1:120108000-120111600	Weak transcription	Right Atrium	heart
9	chr1:120108600-120111200	Weak transcription	Primary B cells from cord blood	blood
10	chr1:120108800-120111800	Weak transcription	Ovary	ovary
11	chr1:120109200-120111400	Weak transcription	Primary B cells from peripheral blood	blood
12	chr1:120109200-120111400	Weak transcription	GM12878-XiMat	blood
13	chr1:120109600-120117200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:120110400-120111400	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr1:120110400-120111600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr1:120110400-120112800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr1:120110600-120111600	Weak transcription	NHEK	skin
18	chr1:120111000-120112400	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr1:120111000-120112400	Enhancers	Fetal Thymus	thymus
20	chr1:120111000-120112800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr1:120111200-120112000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr1:120111200-120112400	Enhancers	Primary B cells from cord blood	blood
23	chr1:120111200-120112600	Enhancers	Fetal Lung	lung
24	chr1:120111400-120112000	Enhancers	Primary B cells from peripheral blood	blood
25	chr1:120111400-120112200	Enhancers	Adipose Nuclei	Adipose
26	chr1:120111400-120112200	Enhancers	Placenta Amnion	Placenta Amnion
27	chr1:120111400-120112400	Enhancers	Primary hematopoietic stem cells	blood
28	chr1:120111400-120112400	Enhancers	GM12878-XiMat	blood
29	chr1:120111400-120112800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
30	chr1:120111600-120111800	Enhancers	Left Ventricle	heart
31	chr1:120111600-120111800	Enhancers	NHEK	skin
32	chr1:120111600-120112000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
33	chr1:120111600-120112000	Enhancers	Fetal Muscle Trunk	muscle
34	chr1:120111600-120112000	Enhancers	Lung	lung
35	chr1:120111600-120112000	Enhancers	Right Atrium	heart
36	chr1:120111600-120112200	Enhancers	Fetal Muscle Leg	muscle
37	chr1:120111600-120112400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:120111600-120112400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr1:120111800-120112000	Enhancers	Ovary	ovary
40	chr1:120111800-120129800	Weak transcription	Left Ventricle	heart
41	chr1:120112000-120112600	Enhancers	HUVEC	blood vessel
42	chr1:120112000-120114000	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr1:120112000-120116400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr1:120112000-120129600	Weak transcription	Right Atrium	heart
45	chr1:120112400-120112800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:120112400-120115400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr1:120112400-120116600	Weak transcription	Placenta	Placenta
48	chr1:120112800-120113800	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr1:120112800-120113800	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr1:120112800-120116600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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