Tag | Content |
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EnhancerAtlas ID | HS002-01141 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:221887610-221889410 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:221889327-221889345 | CCCTCCTCCCTCCCCTCC | - | 6.27 | IRF1 | MA0050.2 | chr1:221888061-221888082 | TTTTCCTTTCCCTTTCTTTTG | + | 6.21 | POU2F2 | MA0507.1 | chr1:221887859-221887872 | TTCATTTGCATAA | + | 6.67 | Pou2f3 | MA0627.1 | chr1:221887858-221887874 | GTTCATTTGCATAATA | - | 6.94 | TFAP2C | MA0524.2 | chr1:221888710-221888722 | TGCCTCAGGGCA | + | 6.18 | TFAP4 | MA0691.1 | chr1:221889033-221889043 | AACAGCTGAT | + | 6.02 | YY1 | MA0095.2 | chr1:221887776-221887788 | CAAAATGGCGGC | + | 6.92 | ZNF263 | MA0528.1 | chr1:221889343-221889364 | CCCCTCCCCTCTCCCTCTTCT | - | 6.02 | ZNF263 | MA0528.1 | chr1:221889281-221889302 | TCTCTCCCTCACCTCTCCTCC | - | 6.2 | ZNF263 | MA0528.1 | chr1:221889332-221889353 | CTCCCTCCCCTCCCCTCCCCT | - | 6.37 | ZNF263 | MA0528.1 | chr1:221889327-221889348 | CCCTCCTCCCTCCCCTCCCCT | - | 7.86 | ZNF263 | MA0528.1 | chr1:221889339-221889360 | CCCTCCCCTCCCCTCTCCCTC | - | 7 |
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| Number of super-enhancer constituents: 14 | ID | Coordinate | Tissue/cell |
SE_04249 | chr1:221887970-221891377 | Brain_Anterior_Caudate | SE_05268 | chr1:221887671-221893218 | Brain_Cingulate_Gyrus | SE_07639 | chr1:221879961-221893689 | Brain_Hippocampus_Middle_150 | SE_08233 | chr1:221888049-221893439 | Brain_Inferior_Temporal_Lobe | SE_09465 | chr1:221887611-221890943 | CD14 | SE_13404 | chr1:221889162-221890771 | CD34_Primary_RO01536 | SE_26005 | chr1:221887429-221893752 | Duodenum_Smooth_Muscle | SE_29951 | chr1:221888433-221889607 | Fetal_Muscle | SE_48429 | chr1:221888539-221889045 | Psoas_Muscle | SE_51295 | chr1:221888458-221891449 | Skeletal_Muscle | SE_52175 | chr1:221888544-221890033 | Skeletal_Muscle_Myoblast | SE_54816 | chr1:221887714-221892890 | Stomach_Smooth_Muscle | SE_63303 | chr1:221886936-221925458 | NCI-H82 | SE_64034 | chr1:221888530-221890155 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 221887766 | 221888016 | chr1 | 221887774 | 221888031 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I221714 | chr1 | 221887582 | 221894075 |
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Enhancer Sequence | AGGGTACAGA AGTCCTCCGT AACGTTTTCC TTTTAATGAA AAGCAGCCCC AAATCATTTT 60 CAACAGAGAG CAGCCTGTAA AGTTGAGCTG CAGACACAGA CAAGCAAACT GAGAGCTCGC 120 ACGTGTGGAT GCCAGCAGGA AAGAATTACC TGCGACTAGA CATGTTCAAA ATGGCGGCTC 180 CATCTTCCCT TCTCTGCCGG CCACGTGTAC AGTAAGGAGC AGACAAGATG GCGCCAGGCA 240 AGGGGAGAGT TCATTTGCAT AATAAGATTA GGGTGGGGTG ACCAGCCTCC CCTGAGTGCT 300 GTGTAAACCT CACACCTGAT CAAACCAATC TGTGAGCCCT ATGTAAATCA GATACTGCCT 360 CCTCAAGCCA GACTATAAAA TCTGGCACAT CCACCACCAG TCGGCCTTTT TCCTCTGGGA 420 AGTCACCTCT CTCTCACTAA AGAGCGAGCT GTTTTCCTTT CCCTTTCTTT TGCCTATTAA 480 ACCTCTGCTT CTAAACTCCT CTTGTGTGTC TATGTCCTAA ATTTTCTTGG TGTGAGACAA 540 CGAACCCCGG TTATTTAACC CAGACAAGGT AGCCACTTCA ATAGTTACTA TTGTTTCTCT 600 CAGATGATGT GCCATTCCCT CCCACCCCAA CGTTAAAAAA AACCCAGCAT TCCAGAAAGA 660 AGCTAATACT TGACAATGAC ACTTACCAAG AACTAAAACA GTCACTTTCG CTACTTCCTA 720 ATCTTTGTAT AATTAGCAGT GTGCTTTCTT CTCCATTTTT TGTTCCATAT ACTTCTACAT 780 TTTCCAGTCA TTAACTTGTT TATTGGAGGG GTCTCTTGTC ATTTTTCTTA TATTTTCGAA 840 TATACTGTTT CCTTCCTTGT TTGATAAAAC CTTTGCCATG CCCTCAATAG GAAGAATTTT 900 AAAAAATTAT TGCCCACATA TTTACCTCAA AAAAGTAAAC TGAGTCAGAA ACATCCAATG 960 ATTTAGGAAT TGTGATTTAT GAAAATTGAA AATAAAGTTT AATTGGAGGC CTTCCAAGAA 1020 ATGCTGACCC TGGAAAGTTT TTGTCAGAGC TTTAAAGATT CCCCTCTGCT CTCACCACCC 1080 TCCCCTCCTG GCTCAGAAGT TGCCTCAGGG CAGAATTGGT ATAGAAAAGA GCTGGGGATT 1140 GGATTTCCGC CGGCTGGAGT AGCTCAGTCC ACACAGAAAA GTCAGCCTCT GGTTCCTACC 1200 CCCTGAAGGG AGGTGCAGTT CTCTTGCCCC CCTCCTACCA TTTCAACTTT AAGGCTTTAA 1260 TGAATAACTA ATGTTTGAGC TACCACAAGT TTAATTTGTG TGTATTTGAA TAACACAGGC 1320 AGATTGTTTT GAGAGGATAC CTCAGAAGTA TGTAAATACA GCCTGTTTCT TTAAATCTGT 1380 TACCTCATTT ATTTACATTA GAACAGAAAG CACTGCCAGA AGCAACAGCT GATGACAGTC 1440 ATGTAATTTT CCACAAAGAC AACAATTAAA CAGCTTTGTG TTATTTTAAT GAGCAGATGA 1500 CTTTTATGTG AGCAGGATTT GAACTGTTAA GATCTCAAGA GTTCCCAGAG CCAGGAAGCC 1560 CCTCAGGTTT TGCAGAAGTC AGTGAGACTC TATGACTCTC TCTGGTTTCT TCCCCACCAG 1620 GGCCTTGGGT TTGGTCTCTA TCTCTATCCC CTTTGCCCCC TTCTCCACTC TTCTCTCCCT 1680 CACCTCTCCT CCCCAACTCT TGCTCCTCTA CCCTGATCCC TCCTCCCTCC CCTCCCCTCC 1740 CCTCTCCCTC TTCTCTCCCT GTCCCTGCCA TCTCCCCTCT TCTACCCTTC TCTCCCTCTC 1800
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