Variant report

Variant	nsv1004343
Chromosome Location	chr1:209879304-209909385
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:165)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:165 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:209901218-209901705	K562	blood:	n/a	n/a
2	ATF1	chr1:209901245-209901423	K562	blood:	n/a	n/a
3	ATF2	chr1:209897398-209897976	GM12878	blood:	n/a	n/a
4	ATF2	chr1:209897289-209897894	GM12878	blood:	n/a	n/a
5	BATF	chr1:209897311-209897669	GM12878	blood:	n/a	chr1:209897567-209897578
6	BATF	chr1:209907067-209907465	GM12878	blood:	n/a	chr1:209907298-209907309
7	BATF	chr1:209897334-209897783	GM12878	blood:	n/a	chr1:209897567-209897578
8	BATF	chr1:209900883-209901057	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:209897328-209897763	GM12878	blood:	n/a	n/a
10	BCL3	chr1:209897327-209897792	GM12878	blood:	n/a	n/a
11	CEBPB	chr1:209906759-209907251	HepG2	liver:	n/a	chr1:209906900-209906911
12	CEBPB	chr1:209906759-209907275	K562	blood:	n/a	chr1:209906900-209906911
13	CEBPB	chr1:209906827-209907085	Hela-S3	cervix:	n/a	chr1:209906900-209906911
14	CEBPB	chr1:209906840-209907055	H1-hESC	embryonic stem cell:	n/a	chr1:209906900-209906911
15	CEBPB	chr1:209906744-209907217	A549	lung:	n/a	chr1:209906900-209906911
16	CEBPB	chr1:209906794-209907193	IMR90	lung:	n/a	chr1:209906900-209906911
17	CREB1	chr1:209897371-209897884	GM12878	blood:	n/a	n/a
18	CREB1	chr1:209894589-209894997	GM12878	blood:	n/a	n/a
19	CTCF	chr1:209898920-209899070	SAEC	small airway:	n/a	n/a
20	CTCF	chr1:209898560-209898710	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr1:209898640-209898790	HMEC	breast:	n/a	n/a
22	CTCF	chr1:209898660-209898810	GM12878	blood:	n/a	n/a
23	CTCF	chr1:209882321-209882358	GM13976	blood:	n/a	n/a
24	CTCF	chr1:209898720-209898870	Caco-2	colon:	n/a	n/a
25	CTCF	chr1:209900971-209901141	K562	blood:	n/a	n/a
26	CTCF	chr1:209898780-209898930	NHEK	skin:	n/a	n/a
27	CTCF	chr1:209898761-209898831	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr1:209898740-209898890	A549	lung:	n/a	n/a
29	CTCF	chr1:209898652-209898922	K562	blood:	n/a	n/a
30	CTCF	chr1:209898580-209898730	NHEK	skin:	n/a	n/a
31	CTCF	chr1:209908640-209908790	Caco-2	colon:	n/a	n/a
32	CTCF	chr1:209898740-209898890	RPTEC	kidney:	n/a	n/a
33	CTCF	chr1:209898700-209898850	RPTEC	kidney:	n/a	n/a
34	CTCF	chr1:209898560-209898710	A549	lung:	n/a	n/a
35	CTCF	chr1:209898680-209898830	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr1:209898720-209898870	MCF-7	breast:	n/a	n/a
37	CTCF	chr1:209898700-209898850	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr1:209898722-209898822	MCF-7	breast:	n/a	n/a
39	CTCF	chr1:209906880-209907030	HMF	breast:	n/a	n/a
40	CTCF	chr1:209898751-209898763	GM10266	blood:	n/a	n/a
41	CTCF	chr1:209898720-209898870	HMEC	breast:	n/a	n/a
42	CTCF	chr1:209898980-209899130	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr1:209899060-209899210	GM12872	blood:	n/a	n/a
44	CTCF	chr1:209898680-209898830	SAEC	small airway:	n/a	n/a
45	CTCF	chr1:209898715-209898793	LNCaP	prostate:	n/a	n/a
46	CTCF	chr1:209908920-209909070	GM12873	blood:	n/a	n/a
47	E2F4	chr1:209885792-209885992	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr1:209890392-209890592	MCF10A-Er-Src	breast:	n/a	n/a
49	EBF1	chr1:209907845-209908078	GM12878	blood:	n/a	chr1:209907960-209907971
50	EBF1	chr1:209894833-209894859	GM12878	blood:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:209898728..209900231-chr1:209914075..209916050,2	K562	blood:
2	chr1:209898273..209898882-chr1:209921133..209921700,3	MCF-7	breast:
3	chr1:209901763..209904735-chr1:209904804..209907749,3	K562	blood:
4	chr1:209901763..209904735-chr1:209904804..209907749,3	K562	blood:
5	chr1:209897489..209898995-chr1:209918699..209920810,2	K562	blood:
6	chr1:209893922..209895818-chr1:210001055..210002815,2	MCF-7	breast:
7	chr1:209887863..209889453-chr1:209910765..209912630,2	K562	blood:
8	chr1:209900061..209902674-chr1:209907942..209909580,2	K562	blood:
9	chr1:209873397..209875484-chr1:209878580..209881106,2	K562	blood:
10	chr1:209879551..209882258-chr1:209882693..209884984,3	K562	blood:
11	chr1:209877047..209878564-chr1:209885238..209887392,2	K562	blood:
12	chr1:209879551..209882258-chr1:209882693..209884984,3	K562	blood:
13	chr1:209900061..209902674-chr1:209907942..209909580,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-G0S2-3	chr1:209894009-209894546	NONHSAT009228
2	lnc-G0S2-3	chr1:209894009-209894141	NONHSAT009229
3	lnc-G0S2-3	chr1:209879773-209879854	NONHSAT009229
4	lnc-G0S2-3	chr1:209880184-209880325	NONHSAT009229
5	lnc-G0S2-2	chr1:209882788-209882832	NONHSAT009227
6	lnc-G0S2-3	chr1:209879660-209880325	NONHSAT009228
7	lnc-LAMB3-1	chr1:209897375-209897470	ENSG00000227591.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HSD11B1	hsa-miR-26b-5p	chr1:209908208-209908228

Variant related genes	Relation type
ENSG00000227591	TF binding region
ENSG00000117594	chromatin interactions
ENSG00000117597	chromatin interactions

Extended variants
information (count: 1074 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1074 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13306423	chr1:209879304-209879305	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370466267	chr1:209879318-209879319	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373588076	chr1:209879324-209879325	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs45473893	chr1:209879333-209879334	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368918427	chr1:209879341-209879342	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576125128	chr1:209879377-209879378	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543629047	chr1:209879388-209879389	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370144465	chr1:209879427-209879428	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562352197	chr1:209879507-209879508	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533213932	chr1:209879537-209879538	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529550096	chr1:209879559-209879560	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11799643	chr1:209879599-209879600	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs184899454	chr1:209879627-209879628	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533129707	chr1:209879632-209879633	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111446354	chr1:209879641-209879642	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370936820	chr1:209879657-209879658	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190187963	chr1:209879659-209879660	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs34205549	chr1:209879682-209879683	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs569799629	chr1:209879705-209879706	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs12040780	chr1:209879846-209879847	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs181887062	chr1:209879888-209879889	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs568205758	chr1:209879939-209879940	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs535292967	chr1:209879984-209879985	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs554078727	chr1:209879985-209879986	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs565994081	chr1:209880002-209880003	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
26	rs549535293	chr1:209880042-209880043	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
27	rs569365044	chr1:209880046-209880047	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
28	rs147231644	chr1:209880058-209880059	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
29	rs368758549	chr1:209880068-209880069	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
30	rs372161445	chr1:209880096-209880097	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
31	rs200402963	chr1:209880129-209880130	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
32	rs142849016	chr1:209880158-209880159	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
33	rs375266448	chr1:209880165-209880166	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
34	rs557818199	chr1:209880212-209880213	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
35	rs576055469	chr1:209880214-209880215	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
36	rs72215241	chr1:209880216-209880217	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
37	rs45487298	chr1:209880218-209880219	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
38	rs12086634	chr1:209880259-209880260	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs371864479	chr1:209880267-209880268	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
40	rs200635241	chr1:209880317-209880318	Genic enhancers Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
41	rs200360270	chr1:209880338-209880339	Genic enhancers Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs578197035	chr1:209880346-209880347	Genic enhancers Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs574132787	chr1:209880348-209880349	Genic enhancers Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs139132286	chr1:209880358-209880359	Genic enhancers Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs387907168	chr1:209880365-209880366	Genic enhancers Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs376208100	chr1:209880366-209880367	Genic enhancers Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs369189519	chr1:209880400-209880401	Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs541250922	chr1:209880430-209880431	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs371896771	chr1:209880447-209880448	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs376494402	chr1:209880457-209880458	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	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
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
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
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
Breast cancer	21611746	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:209870800-209880000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:209870800-209880200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr1:209875200-209882400	Enhancers	Brain Substantia Nigra	brain
4	chr1:209877400-209882600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr1:209878200-209879400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:209878400-209880800	Weak transcription	Brain Germinal Matrix	brain
7	chr1:209878400-209881800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr1:209878600-209879400	Enhancers	Brain Hippocampus Middle	brain
9	chr1:209878600-209881200	Weak transcription	Brain Anterior Caudate	brain
10	chr1:209878600-209881400	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr1:209878600-209888200	Weak transcription	Brain Angular Gyrus	brain
12	chr1:209878800-209880400	Weak transcription	NHLF	lung
13	chr1:209878800-209893400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:209879000-209881400	Weak transcription	Brain Cingulate Gyrus	brain
15	chr1:209879200-209879400	Enhancers	Adipose Nuclei	Adipose
16	chr1:209879200-209879600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:209879200-209879600	Weak transcription	Ovary	ovary
18	chr1:209879200-209880400	Flanking Active TSS	Liver	Liver
19	chr1:209879400-209880000	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr1:209879400-209880800	Weak transcription	Brain Hippocampus Middle	brain
21	chr1:209879400-209881000	Weak transcription	Adipose Nuclei	Adipose
22	chr1:209879600-209880600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:209880000-209880600	Enhancers	Gastric	stomach
24	chr1:209880000-209881000	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:209880000-209881200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:209880000-209881400	Enhancers	HMEC	breast
27	chr1:209880200-209881000	Enhancers	HUVEC	blood vessel
28	chr1:209880200-209881400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:209880200-209881400	Enhancers	NHEK	skin
30	chr1:209880200-209881800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:209880400-209880600	Transcr. at gene 5' and 3'	Liver	Liver
32	chr1:209880400-209881000	Enhancers	NHLF	lung
33	chr1:209880600-209881200	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:209880600-209883800	Genic enhancers	Liver	Liver
35	chr1:209880800-209882200	Enhancers	Brain Germinal Matrix	brain
36	chr1:209880800-209882400	Enhancers	Brain Hippocampus Middle	brain
37	chr1:209881000-209883200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:209881000-209885200	Weak transcription	HUVEC	blood vessel
39	chr1:209881200-209881800	Enhancers	Brain Anterior Caudate	brain
40	chr1:209881200-209882800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:209881200-209886000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:209881400-209882600	Enhancers	Brain Cingulate Gyrus	brain
43	chr1:209881400-209883000	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr1:209881400-209883600	Weak transcription	NHEK	skin
45	chr1:209881400-209884600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:209881400-209887200	Weak transcription	HMEC	breast
47	chr1:209881600-209882000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
48	chr1:209881600-209882000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr1:209881800-209882000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr1:209881800-209882200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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