| Tag | Content |
|---|
EnhancerAtlas ID | HS095-07663 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:96622420-96623890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr12:96623665-96623678 | ATGACCTCATCTT | - | 6.54 | | JUND(var.2) | MA0492.1 | chr12:96623664-96623679 | TATGACCTCATCTTA | - | 7.07 | | Mecom | MA0029.1 | chr12:96622672-96622686 | AAGAGAAGATAAGA | + | 6.13 | | Myod1 | MA0499.1 | chr12:96622579-96622592 | TCCAGCTGTCCCT | + | 6.16 | | Nr2f6(var.2) | MA0728.1 | chr12:96623528-96623543 | TGAACTCCTGACCTT | - | 6.04 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_35865 | chr12:96622065-96624273 | HMEC | | SE_37993 | chr12:96622087-96623497 | HUVEC | | SE_44155 | chr12:96622201-96623307 | NHDF-Ad | | SE_44155 | chr12:96623371-96624515 | NHDF-Ad | | SE_44822 | chr12:96622479-96623040 | NHLF | | SE_45717 | chr12:96622132-96623435 | Osteoblasts | | SE_64664 | chr12:96622180-96623440 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I096228 | chr12 | 96622325 | 96623819 |
|
Enhancer Sequence | GCTGTGAAGA TGCTTTCTTA TTTAAATGAC TCTCCCTCAC CGCTCTGAAT CAAAGCTCTG 60
GCACTTCTCT GAGCACCTGC AGTTGGAGCC AGTCTCCACC TTCTGGACTG TCTTAGTGAC 120
TGGTGGGAGC TTTGTATCCA GAGCCCTCGA GGTTAAGAGT CCAGCTGTCC CTCAACCTCA 180
GCGTCTCAGT TCACCCATTG GAAAGTGGTG ATGGGAACAG CACCCTTCCT TGTCGGACTG 240
TGTGAGGATG GAAAGAGAAG ATAAGATGAC GCGGATAAGG TGCTTAGCAC AGTGTCAGGC 300
ACCTACTCAG TGAAGGCTCC TCATTCCAGT TATGTGTATT TATAAAACTG ACTGTATTAT 360
GTCGTAGCTG TCTGTATATA GCTGACTTCA TCGTGGCCTT CTGGATGCAC CACTTTTGTC 420
GCTCTGGTAC CTCGGACAGG GTCTGGCATG TATTAGTTGC TTAGTAAATG CTAGACGAGT 480
GAACAAATGG ATAAAACACT GATGTGTCCA CTACTCAAGT GCACACCATT TATGTCATGA 540
AAGTTGATAT TAATGAGTGA TAAACTAAAA AATAAAAGTA GTCACTGCTT TTTGTTTATT 600
GTCCCGTAGT TTCCTAGGGC TGCCAGGTCA GATGACCACA AACTGTAGGT GGCTTAAAAC 660
AACAGAAATG TGTTGTCTCA CAGTTCTGGA GGCCAGATGT CCAGAGCCAG GGTGTCAGCA 720
GAGCTGTGCT CCCTCTGACT CAGGTGGACT CTTTCTTGGC CTCTCCCCAG CCCCGGGCTT 780
GCCAGCAGTC CCTGGCGTGC CTTGGCTTGC AGCAGCCTCA CTCGGATCGC TGCCCCCATC 840
ATCACATGAC GTTCTCCCCA TTCTGTGTGT CCAGATTTTC CTTTTTTTTT TTTTTTTTTT 900
TTTTTTTGAG ACAGAGTCTT GCTCTGTCGC CCAGGCTGGA GTGCAATGGC ATGGTCTCAG 960
CTCACTGCAA ACTCTGCCTC CCAGATTCAA GGGAGTCTCC TGCCTCAGCC TCCTGAGTAG 1020
CTGGGACTAC AGGCATGTGC CACCACACCT GGCGAATTTT TGTGTTTTTA GTAGAGATGG 1080
GGTTTCAATA TGTTGGCCAG GCTGGTTTTG AACTCCTGAC CTTGTGATCT GCCTGCCTCA 1140
TCCTCCCAAA GTGCTGGGAT TACAGGTGTG AGCCACCGTG CCTGGCCGAT TTTCCTCTTC 1200
TTATGAGGAT ACCGGTCATT GGATTAGGGC CCACCTTAAT GCATTATGAC CTCATCTTAA 1260
CTTGGTTACG TCTGTAAAGA CCCCTTTCTA AATAAGGTCC TAGTCACAGG TATTGGGGAT 1320
TAGGACATCA GCATAGTTTG GGGAAGGACA AAATTCACTC TGTAACACCT CCATATACAG 1380
TCATGTACCA CATAATGTTC TGGTCCACAG TGGGCCACGT ATATAACAGC GGTCCCATAA 1440
GACTATAATT CCATATTTTT ACTGTACCTT 1470
|
