| Tag | Content |
|---|
EnhancerAtlas ID | HS081-12708 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr21:44937590-44939140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYB | MA0100.3 | chr21:44938860-44938870 | ACCAACTGTC | + | 6.02 | | PBX1 | MA0070.1 | chr21:44938964-44938976 | TTTGATTGATGT | - | 6.74 |
|
| | Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
| SE_23553 | chr21:44932094-44938632 | Colon_Crypt_1 | | SE_24270 | chr21:44933912-44937905 | Colon_Crypt_2 | | SE_24764 | chr21:44933892-44938636 | Colon_Crypt_3 | | SE_27259 | chr21:44929167-44938707 | Esophagus | | SE_33898 | chr21:44934265-44941366 | HCC1954 | | SE_34698 | chr21:44935647-44938978 | HeLa | | SE_35943 | chr21:44934281-44943674 | HMEC | | SE_36970 | chr21:44934685-44938656 | HSMMtube | | SE_51730 | chr21:44935825-44937908 | Skeletal_Muscle_Myoblast | | SE_58009 | chr21:44937539-44937846 | VACO_9m | | SE_58009 | chr21:44937851-44938441 | VACO_9m | | SE_63514 | chr21:44935697-44937842 | HSMM | | SE_64394 | chr21:44935482-44939379 | NHEK |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH21I006020 | chr21 | 44935646 | 44938445 | | GH21I043509 | chr21 | 44929453 | 44943529 |
|
Enhancer Sequence | CTTCTGGGCT CATGGGAGAG GTGCAGTCAC AGTGCCCTCC TGCCCCCTCA TACACGGGGG 60
TGCAGAGCCA GAAGCAAATG GGAGACAAAC ATTCCCCTAA ACCCTAGTTC CAGCCCACAC 120
AGCCAAAAGC CAACTCCCCC TTAGAAAACC TTAGTATGCG TGTCAGCCAA ATTCCTTAGG 180
GTTGAGGCAG AGGTGTAGCG AGGGAAGCTT GCCGGACTAG AGTCAAGACA CAGGTATGTT 240
TAGCATGGGA AGGAAGGTAT GACAGTCCCC ACACACAGAG ACGCAGACAG AGAGAGAGAT 300
GCACACAGAG ACACACAAAA ACATACAGAC AAGATACAGA AACAACACTC ACAGGCACAG 360
TCACACAGAC ATACATGCAC ACATACATGC AGACTCATAC AGATAGGCAC ACACAGAGGC 420
ACAGTCACAC ACAAAGACAC ACACACACAC ACACACACAC ACACACACAC ACACAGAGAC 480
AGACACAGAT CTGTGGTCAT CTCCACTGAA TTGCCAGGGA CATCACTGAA ACAACTTGAA 540
CTCTGTCCAC ACCTGATTCA GGCAATAAGT GTCTGTGGGT CAGGGCAGGG GTTATGGGTG 600
GATCCCACCG TGGTGTGACT GTGGGGAGAG TCCAGGGCAG CTCAGCAGCC TCCAGGGAAG 660
GACACAGCCC AGGAGAAGTG CTAGGGGAGT CTGGGGCCCT GGTGGGTGGC TTGGACAGGT 720
AGTGGGAGCA GCACCCAAGG AATACGGAGG CCCAACCAGT TGAGTGGCAG AGGCTCTAGC 780
CAGCCTGGGC ATGGGTGCCT TTTCCACCCA GGGTAAACTG CAGCCACAGG GGCAGGGGTC 840
CCCGAGGAGA AGGCGGCACA AGGAAGGGCT CTCAAGGCAC CTTCTTGAAG ACCAGGAAGA 900
CTTTGTGAAA GGAAAATAAA TCTCGGGACC CCAAAATCAC TAAGCCAAAG GGCAAAGTCA 960
AGCTGGTGTA AACCAAAAAT AAAATTCTAA GTCCCCCGAC AAGAACGGAC CCTTCCTCTC 1020
AGCAAGGGCA TTCCAAAGCT AACCTGAAAA ACAAGTTCAG GCCATGATGG GAAGGGAAGT 1080
CAGGCATGAC TCATTATACC CTCTTCCCTT TTGGAATTAC TGATAGAATA GGGTCTTTAA 1140
GTCTGATAAG AAACATTTAC AATCTATTGT CTCCGAAGCC TGCTACCTGG AGGCTTCACC 1200
TATGGTCTCC ACAAACCCTT ATCTTAACCC AGACATTCCT AAGTCTTTAG ACAATAACTT 1260
AACTCTTTCA ACCAACTGTC AATCAGAATA TCTTTGAATC TACCTATGAG TTGGAAGCCC 1320
CCACCTTCCA GTTGTCCCGC TTTTCCAGAC CGAACCAAAG TACATTTACA TGCATTTGAT 1380
TGATGTCTCA TGTCTCCCTA AAATGTACAA GCTGTACTCC ATCCACCTTG GATACATGAT 1440
CTCAGAACCT CCTGGGGTTG TGTCATGGGC CACTGGTCAC TCATATTTGG CTCAGAATAA 1500
ATCTATTCAA ATATTTTAGA GAGTTTGACT CTTTTTGTTG ACACTGGGAA 1550
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