| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08411 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:105608380-105609740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr12:105608441-105608457 | CTTGGTCTTTGACCCC | - | 6.22 | | KLF16 | MA0741.1 | chr12:105608603-105608614 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr12:105608603-105608613 | GCCCCGCCCC | + | 6.02 | | SP1 | MA0079.4 | chr12:105608600-105608615 | TTAGCCCCGCCCCCA | + | 6.76 | | SP2 | MA0516.2 | chr12:105608599-105608616 | TTTAGCCCCGCCCCCAT | + | 7.14 | | SP4 | MA0685.1 | chr12:105608600-105608617 | TTAGCCCCGCCCCCATC | + | 7.35 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27994 | chr12:105606751-105611626 | Fetal_Intestine | | SE_28891 | chr12:105606562-105611807 | Fetal_Intestine_Large | | SE_44294 | chr12:105604391-105609501 | NHDF-Ad | | SE_45950 | chr12:105604150-105610743 | Osteoblasts |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I105210 | chr12 | 105604459 | 105611375 |
|
Enhancer Sequence | TCTGAAAACC CTTGTAATTT CCTCATCAAT AGAAGTGCTA GGAGCATATT TTGTTATAAT 60
ACTTGGTCTT TGACCCCAGT TTCTGACACA GAGATCCTAA TCCTTTGGAA TTTCCTGGAT 120
GATGGGAGTG TCTTTTGTTC TGATGAGGCA ACTCCTGGTG GCCTCCAGGA TAGGGGCTGG 180
TCACCAGAAA CACCAAACCA CGATTATGAG CTTGGAGCTT TTAGCCCCGC CCCCATCTTC 240
CAGGAACGGG AGAGAGCTGG AGGTTGATCA CATCTATGTG ATGAAGCTGC CAATAAAAAT 300
ACCTGAACTG CAGGGTTTGG AGAGCTTCCA GGTCATTAAA ACACCTGGCA GAGCCCAGAG 360
GGGTGACGTC CCCAGAGAGG GCACGGAAGT TCCACGCCGC CTCCCCTGTA CCTTGCCCTA 420
TGTATCACTT AATCTGGCTG TTCATCTGTG TCCTCTGTAA TATCCTTTAT AATAAAGGTA 480
AATTTAAGTG TTTCCCTGAT TTGTGGGCCA TTCTAGAAAA TAATCAAATC CCAGGGGGAT 540
GTTGCAGGAA CCCCTAGTTT ATAGCTCGTT TGTCAGAAGT ACCAGAGGCC TAGACTTGCA 600
ATTGGCATCT GAAGTGTGGG GGAGGGGGTA GTCTGGCGGG ATCATGCCCT TAACTTGTGG 660
GATCTGAGGC TATCTCCAGG TAGATATGTC AGAATTGAGT TAAATTGTAG GACAGCCAGT 720
TAGTGTCACA GAATTGCTTG ATGTGGGGAA AACCCACACA TTTTGGTGAC CAAAGTGTGC 780
TGAGTGCTGA AAGTATAGAA AGAGAATGAG TTTGTCTTTT TCCTACTGTT TAGTAGGGTA 840
GAGGACAAAG CCCAATAAAA ATCATATGAC GTGTTCACTT TTACATCCCC CGTGCCTAGA 900
ACAGCGTCTG CTAAATAGGA GGTCATCAAT AAATGTTTGT TGAATAAATA ATGGCTTGTT 960
GAACTGGTTT GTTGAATAAA CGAAAATGCA ATCAGTACAG TTTTATATGA ATGTTAGTTT 1020
CTCATTTTGT AAACTGAAGA CAGTATCTAC TGCAGATCAA TAACTGGTCA GTTAAATGGC 1080
ATCTGCACAC TCCTTTATGT TTATTCTTTA TCATGATTTT TTGAGTATTC AAACTCCTTA 1140
AAAGATGGAA CTATTTGGCC AGGCGCGGTG GCTCATGCCT GTAATCTCAG CACTTTGGGA 1200
TGCCGAGGTG GGCGGATCAC AAGGTCAGAA GACCGAGACC ATCCTGGCCA AGATTTTTAG 1260
TAGGGTGAAA CCCTACTAAA AATACAAAAA ATTAGCCGGG CGTAGTCCCA GCTACTCGGG 1320
AGGCTGAGCC AGGAGAATGG TGTGAACCCG GGAGGTGGAG 1360
|
