| Tag | Content |
|---|
EnhancerAtlas ID | HS175-02874 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr1:223925430-223928000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr1:223927699-223927711 | GAAATCACTGCA | + | 6.74 | | Nkx2-5(var.2) | MA0503.1 | chr1:223926788-223926799 | AGGCACTCAAG | + | 6.14 | | Nr2f6(var.2) | MA0728.1 | chr1:223927104-223927119 | TGAACTCCTGACCTC | - | 6.22 | | RORA | MA0071.1 | chr1:223927759-223927769 | TGACCTTGAT | - | 6.02 | | STAT3 | MA0144.2 | chr1:223926464-223926475 | CTTCCCAGAAG | - | 6.14 |
|
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_00224 | chr1:223925520-223928901 | Adipose_Nuclei | | SE_01908 | chr1:223926095-223926935 | Aorta | | SE_01908 | chr1:223927075-223928148 | Aorta | | SE_09681 | chr1:223926086-223926867 | CD14 | | SE_23408 | chr1:223924747-223925696 | Colon_Crypt_1 | | SE_23408 | chr1:223925806-223926930 | Colon_Crypt_1 | | SE_23408 | chr1:223927008-223928133 | Colon_Crypt_1 | | SE_24051 | chr1:223926231-223926878 | Colon_Crypt_2 | | SE_24051 | chr1:223927084-223928100 | Colon_Crypt_2 | | SE_25230 | chr1:223926296-223926903 | Colon_Crypt_3 | | SE_25230 | chr1:223927114-223928239 | Colon_Crypt_3 | | SE_26209 | chr1:223926103-223928290 | Duodenum_Smooth_Muscle | | SE_26925 | chr1:223926095-223928145 | Esophagus | | SE_31491 | chr1:223923671-223928232 | Gastric | | SE_33950 | chr1:223925357-223926983 | HCC1954 | | SE_33950 | chr1:223927048-223928269 | HCC1954 | | SE_34545 | chr1:223926186-223927072 | HCT-116 | | SE_36294 | chr1:223927044-223927974 | HMEC | | SE_37129 | chr1:223924560-223926499 | HSMMtube | | SE_37129 | chr1:223926584-223928521 | HSMMtube | | SE_38254 | chr1:223923616-223925758 | HUVEC | | SE_41495 | chr1:223927102-223928062 | Left_Ventricle | | SE_42269 | chr1:223925796-223927012 | Lung | | SE_42269 | chr1:223927049-223928176 | Lung | | SE_50365 | chr1:223925795-223926977 | Sigmoid_Colon | | SE_50365 | chr1:223927008-223928158 | Sigmoid_Colon | | SE_53249 | chr1:223926157-223926979 | Small_Intestine | | SE_53249 | chr1:223927086-223928250 | Small_Intestine | | SE_64794 | chr1:223926064-223928210 | NHEK | | SE_65644 | chr1:223924602-223925734 | Pancreatic_islets | | SE_65644 | chr1:223925909-223927309 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 223925467 | 223925641 | | chr1 | 223926096 | 223927104 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I223736 | chr1 | 223924574 | 223930136 |
|
Enhancer Sequence | ACAATAACAC CATGTACTGT AAAGAAAAAC AGTCAGTTCT AAAAGAAAAA CAACCCAGAA 60
AGAAGGGAAT GTGTCAAAAC CGGGAGAGGG GAAAAAAAAA GGCATGCATG CTTTCAAAAG 120
CACCTTAGGG GCTACAGATG GGCCCTATAC TTAGTGTTGA CACCCAACAG CCATAAAAGA 180
ATCTCACTGT GCCCCCAGGG GAGCACAGGG AAGGTCTGAT TCTAGATTTT TTCTGTGCCA 240
TTTATTTATC TATATCCTCA TGCACAAGTT CTATACTGTT TTAATTGCTG TAGCTTTTTA 300
TGTGTTTAAA CATCTAATAG AGGTAGACTT CCTTCTCTTA GATTTTTTTC TAGCTATGCT 360
TCATATTTAA TTTTTAAATA AACTTATCAG AATCAGCTAA GTTCAAAAAC AATTTTTAAT 420
CTTATTACCT TTTTTTTTCT TTTTTGTGAG ACGGGGTCTT GTTCTGTCAC CCAGGCTGGA 480
GTACAGTGGT ACAATCATAG CTCACTGCAG CCTTGACCTC CCAGGTTCAA AGTGATTCTC 540
CTGCCTCAGC CTCCCAAGTT GCTGGGACGA TAGAAGCATG ACACCACACC TGGCTAATTT 600
TTTAAAAATA ATTTTTATAG AGACAGGGTC TCACAGTATA GTGAGATTTC AGGGTGGTCT 660
TGAAATCCTG AGGGCTCAAG AAATCCTCCA GCCCTGGCCT CCCAAGAGCT AGAATTACAG 720
GCATGAGCCA CCGTACCTAG CCCTATTGCT ATTTTTATTA GCATTACATT AAGTTTATAG 780
GCTAACTTAA GAGGACATGG CATTTTTATG ATAATGAGTT TTTGCAGTCA AGAACGCAGG 840
CCAGTTTTTT TTAAATGGGG TAAATGATTG TCCAAGCGCC TCCAGGCAGG CTCACGTGCA 900
CACTCTGGAG TCAGTGAAGA AGGTGAACAG CTGACAGGAG CAGCCTCCCA GTCAGAGAAG 960
CCCTGCACAC TGTTGCAAAC AGACAGCTTG CATCTGGAGT CTTCTGTGAT CCGAGGAGGA 1020
AGCGTGGCTG AGTCCTTCCC AGAAGAGGGT CTGGAGCTGT GAGTTGGGGA CAATTGTCAG 1080
ATTCTAGCAG TGAAAGTGGT TCATGTGCAG GTGCAACCTG CCCCGCAGTC ACGGGACACA 1140
GCCACATGGA GCCGAGCCAC GCTCTCAGAG AAGGAGCCAG GGAAGAAACA CCCTAACTGC 1200
ACTCCTCCCT TCTTCTGGCC CCCAGCAGCC ATAGGCCCTG GGCCCCCGGT GAGATACCCA 1260
TAGAGATCAG CTCCCAGGCA GCAGGATGGA GGGTGTAGAC TGGACATGAA GAGGCAGCTG 1320
GAATGTATCG GGCACTCAGC TCCAGCTCAC CACGATCCAG GCACTCAAGT TCCCAAGACA 1380
ATAGTTTCTG CTCTCAGATA AATGGAATAA TTAAGGATCA AAAGGTTATC AACAGGTAAC 1440
CAAGCATAAA CAGATTTTTT TTTTTTTTTT TTTTAGACAG AGTCTCACTC TGTGCCCCAG 1500
GCTGGAATGC AGTGGTGCAA TCTGGGCTCA CTGCAACCTC CACCTCCCAG GTTCAAGTGA 1560
TTCTCATGCC TCAGCCTCTC CAGTAGCTGG GACTACAGGC GCGTGCCAAC ATGCCTGGCT 1620
AATTTTTGTA TTTTTAGTAA AGATGGAGTT TCACCATGTT GGCCAGGCTA GTCTTGAACT 1680
CCTGACCTCA TGTGATCTGC CCACCTCGGC CTCCCAAAGT GATGGGATTA CAGGTGTGAG 1740
TCACCATGCC TGGCCCATAA GCAGATTTTG TACCTGAGCA GGAAGGCTAA GAGCTTGTAA 1800
CAACTGAACA TTCCCCCCGG AGAGGAAGGC AGGAGTTTTG CTTGTGCCAA GTGCACTGTT 1860
CAGACAGTCC TCTGAGGTAC ACCAAGGTCT GAGTAGCCAT CCCACCCTCC CCTCTGCCAA 1920
AATTTTTGTG TGACTGGAGA GCAGAGCCCT CCTCCAAAAA TAAAATGAGC ACAAGGAAAA 1980
TACTATTTGC AGATACATAA TATTAAAACC ATAGGTCTTT CTTTTTCTAG TCCCATCCAT 2040
ATGGCAACAT TCCAGGAGAG GCCTCCGTCA CTGGAAGGCA CCCTCAGGGG CTTTCCTGGA 2100
GCTAAAAACA GTTTAAGCCA AAAGTTATTT GTAGCATCTG AGTTAAACTC TTCGTCTCAC 2160
CCTTCTCGAG CTAGCTGGCT TATTTTATCC GGACCAGGAT ATAACAGCTC TAAACAGGCT 2220
TTGCCAGGAA GAGACGTCAT GGACTTCAAC CAGGGCACCT GACCAGGAAG AAATCACTGC 2280
AGGATGATCT GAAAGAGTTT TCATAAATTA TTTTACGTAA GGTAGATTCT GACCTTGATG 2340
GGGACAGCCA AGGTTCTGGA CCCTCAGCTG GGAAAGATGG GACTAAGTCT ACAACTGCTG 2400
AGGTTGTAGA ACAGGCTTCT TGTTGGGAGG AACCCTCTTG TGGACATGGG CCGTCGAGGT 2460
GGAGTGAGAG AACACCGTGC CACCTGGACG CTGAAACACC ATTGAGTCAC CTCTGTTTGA 2520
AATGCTTGTT CCCTGGTGCC GTAAAGAAAT AGCACTTGAA CATAAATTTA 2570
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