| Tag | Content |
|---|
EnhancerAtlas ID | HS044-12777 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr8:48265620-48266720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr8:48266326-48266343 | AAGAACACAGTGTTCTG | - | 6.13 | | Ar | MA0007.3 | chr8:48266326-48266343 | AAGAACACAGTGTTCTG | + | 6.54 | | NR3C1 | MA0113.3 | chr8:48266326-48266343 | AAGAACACAGTGTTCTG | - | 6.23 | | NR3C1 | MA0113.3 | chr8:48266326-48266343 | AAGAACACAGTGTTCTG | + | 6.54 | | NR3C2 | MA0727.1 | chr8:48266326-48266343 | AAGAACACAGTGTTCTG | - | 6.28 | | NR3C2 | MA0727.1 | chr8:48266326-48266343 | AAGAACACAGTGTTCTG | + | 6.53 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_09525 | chr8:48263813-48269233 | CD14 | | SE_27599 | chr8:48264868-48266626 | Esophagus | | SE_36331 | chr8:48264477-48272342 | HMEC | | SE_64835 | chr8:48264643-48272634 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I047351 | chr8 | 48264317 | 48272499 |
|
Enhancer Sequence | AAAAAAAAAA AAAAAAAAAA AAGTTATTCT TTCCAAATAT GATACAATTT TGTTCAACTT 60
AATTTTGTTA AATTTTTATT CAAAAAGTTA AGTTCTAAAT AGCATCAAAC ATGGTGGGAG 120
TCAAAATAAT TAAAATCGTA TTTTTTCTGA AAGTGTGTAG ACTGCCTGCA TACTTATATA 180
TACGCCAGAT TGTATTTTAC TTACCTTCTC ATTTGCATCT TACCCTTGTG GCCGAATTAG 240
CAGGACCTGT GTGAGAATGA CATAACTTCA CCGCCTCTTA CCTGCTCCAG CTGCAACGCG 300
TGAGAGTGCT GAACTGTGGC CTAGATTTTT CTCTAGGGCT TTCCACGGAA GTGAGTCAAC 360
ACATTGTTTC TGGCTTTTCT TGCTGTCCCT CCCTAATATG CAAGCTTAGG TTGCTTTGGA 420
ATTTTCCAGG TACAGTGTTG GAGAAGTTGT AACACAGGAG GAGGCCAGAG CGTAGGTTTA 480
GTGTGGTGGG GAGAGGGTTG GAGCAATTGT TCAAGGGAAG ATTGAAAGTG ACCAAAATGG 540
CATGAGGGTA AAAATGTTAC CTGAATTAAA TATGTACCAA ACACTGAAAA TCCCTTATTA 600
TATTTTAGTA TCTTTTATCA TTGTATTTTA AAATTGATTT AAATCTATAC TGAGATTTTT 660
TTTTTTTTTT TAGTGTGGAT TTCAACACAT TTTTTGTGCT TTTGCCAAGA ACACAGTGTT 720
CTGTTAAGTC ATTCAGTGAC GAAGATTGCT GGATTGCTGC CAGCCCGGGT CAAGTTCATT 780
CACATAAGTT TCAGTGTAGA TTCTGACTGA GTGAGGAATG TTCCTCTTGT CTTTGCATGT 840
TAGGTGGGTC TGGGAAATCA GTTGTTTTAA AACAAGCTTA TTAATACTTT TGTTTTTTTC 900
AGGGTTATGG GGTTTTTTTG CTTTTAAGGC TTCATATACA GACAACGCTT TGATACTAGT 960
ATCACATTCT TGTCTATTTA CTGATTTTCC ATGCCTGATT TGGTGAAATA ACAGCTCTCC 1020
TAACCATACC AGATTAGAAT CTACCGTATA ACGTATTGAC TCTGCTGTAT CATTTTAAGG 1080
TATTATTTTA TATCTTTAAA 1100
|
