| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06002 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:89769340-89770660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr12:89769349-89769364 | TGATCTCTTGACCTT | - | 6.93 | | Zfx | MA0146.2 | chr12:89769372-89769386 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_25078 | chr12:89769520-89771196 | Colon_Crypt_3 | | SE_27644 | chr12:89763300-89771362 | Fetal_Intestine | | SE_28566 | chr12:89761572-89775819 | Fetal_Intestine_Large | | SE_35929 | chr12:89761762-89771214 | HMEC | | SE_38298 | chr12:89761862-89771214 | HUVEC | | SE_41177 | chr12:89769445-89770050 | Left_Ventricle | | SE_50215 | chr12:89769308-89771985 | Sigmoid_Colon |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I089368 | chr12 | 89761900 | 89775589 |
|
Enhancer Sequence | GGATGGTCTT GATCTCTTGA CCTTGTGATC CGCCCGCCTC GGCCTCCCAA AGTGCTGGAA 60
TTACAGGCGT GAGTCACTGC GCCCGGCCGG AAGTCCTTAG TTCTTATAGA TGATTGTTCA 120
GTGTCTTGCA CAATTTTGCT ACTGCCTTAT TTTCCTGCAG ATAAGACATT GTAGTTATGG 180
GTGTTACTGT ATTTATTGGT TCAAAAGACA TGGTGCAAAG GACAAGTAGG CCAAGCAGGC 240
TCTGACTCAT AGAGGTTGCT GCCTGCTTGT GCCCTGTGTG CGCCTTTTGA GTAAAGAGCA 300
CAGTCCACCA AGTCCAGCTC TGCATGCTCA AGTGCTATTG AATTCTTTCC ACCTGACCAC 360
AAGTACTTGA GCACCTTTCC TCCATAGCAG AGCTGATAGC ACAGAGCACA CTGAGAATCC 420
CTATAGGGAA GGTGTGGTGA GGCTGTGTGA ACTGTGTGGG CTGTGGTCAC GTAGTTGATC 480
ATGTAAGTGG GATCACAAAC TTAGTAAGCA TCCTGTGACA CACCGTCATC ATTAGAGTGT 540
GCTTGTTGAT GTTGGAGTAC TATGTGCTAT TCAGGACTAT TTCCAAGAAT TTAGTTGAAT 600
ATATATCCTG GGCTGTAGGA TACAGGATGA AAAGAGGATT TGGTGTCCCT GCCAAGTTTC 660
CTAGATAATG CAGATAATTT CTTTTAGCAG GAAGTGACGT GTACATCTCA GGGCTGGGAA 720
GGTGCAGTTA TAGGAAATTA GCCTTAGCAA GAAACAAAAT GCCAAAATCA AGACCAAGTG 780
AGAACATAAC TTCTAGACCA ACAGAAAGGA AGTGAGGGGA TCTGAGCTGC CCTGTTTTGT 840
TTCTGAAAAA CCACTCATCT TGCTCTTCTA TATTCCTGAC TTTCTCCATC CAGTAGGCAC 900
CAAGTCCAGC TAGCTCTGTC TCTTCTGATT TTGGAATCTG TCTTCCCTTC ACCATCTCTC 960
CAGTCATGGA GTTCAGTCTC TTACCATACT CACCTGGATT ACTGCAATAG ACACTAACTG 1020
GTCTCCCTGC TTTCAGTCTT CAACACCCCA TATCTCACCA AAGGGATCTT TGTTGTCTGT 1080
CCATTGTTAA ATGGTTGGGA TTTATTGGGA GGATTTCTGT CTGCTCTCAG GATGGACCAG 1140
AAGTTTCAGA AATTGATAGA AATGGGTCGG GTAGGGATGG GTAGGGTTAG AACATTCAAC 1200
CGTGTTGTCA GTGCCCTGCC CCAGAATGAA TGCTCTTCCA TCATTTCTCC ATCTTTTCAC 1260
CCTCTTTCTT CACTCCAGGG AGTGAACATT GTTCCAGCTT GGGTCAGGTG GCTGTTTGTT 1320
|
