| Tag | Content |
|---|
EnhancerAtlas ID | HS044-05863 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr17:59312270-59313810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr17:59313004-59313019 | TGACCTTTTCACCTT | - | 6.69 | | RARA | MA0729.1 | chr17:59313001-59313019 | TTTTGACCTTTTCACCTT | - | 6.12 | | ZNF263 | MA0528.1 | chr17:59313075-59313096 | GGAGAAGAAGGAGAAAGAAAG | + | 6.09 | | ZNF263 | MA0528.1 | chr17:59313072-59313093 | AAAGGAGAAGAAGGAGAAAGA | + | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_43427 | chr17:59307431-59315690 | MCF-7 | | SE_46342 | chr17:59312653-59313808 | Osteoblasts |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I061235 | chr17 | 59312453 | 59314055 |
|
Enhancer Sequence | CGGAGTCTCG CTCTGTCACC CAGGGAGGAG TGCAGTGGCA TGATCTCGGC TCACTGCAAC 60
TTCCACCTCC TGGGTTCAAG CAATTCTCCT TCCTCAGCCT CCCGAGTAGC TGGGACTATA 120
GGCGCACGCC ACCACTCCTG GCTAAGTTTT GTATTTTAGT AGAGACAGGG TTTCACCACA 180
TTGGCCGGGC TGGTCTCAAA CTCCTGACCT AAGATGATCC GCCCACTTCG GTCTTCCAAA 240
GTGCTGGGAT TATAGGCGTG AACCACCACG CCTGGCTGTC TGCCCCCCGC CTGTCCTAAG 300
CACTTTAAAT GTGTCAACTC ATTTGGTCTC TTTGAAAAGA GTGGCCAGGT GAAGGCTGAA 360
GGACCGGATA AGTGTAGTTT CCAGAATCCT TCTTGGCTAG TTATAGTCTA AGACTTGCAG 420
ACAGGCAGCC TGGGAAGATC TCAAACAAGT AACCTTCAAT GAAAATGTAC AGTTTTGAGA 480
ATTTCGATAT TTGACAGATG ATTGAGCCAC TCGAGTTGCT TATGCATGAA TGTGCTTGTT 540
TAGCAGGTAG AGTTATTATT CTCTTATGTT CAAATTTATT AACAAGGGCT TAATTTCATT 600
CCAAACAGAT TGTGAGGTGA CTACGTAGTA CAGAAGTACA GTGAAATATG AGATTCCTGA 660
GCCTTTAGTG GATGCTGAGC TGGAGACCCC CGTTAGTGCT ACCTCTTTCT AAACAGCGCC 720
AGCCATGAAG CTTTTGACCT TTTCACCTTT AAACTTTGTT TGAACTTGGA AAGAAGACTT 780
TTGAATTGTT TAAAAAAAAA AAAAAGGAGA AGAAGGAGAA AGAAAGACAA GGGAAAAAAA 840
TGGTTAGGGA GGCTGCAAAA GAGATGTGGA GACTGGGGGA AAAGGACTGA TTATATGTTA 900
GCTTAACAGT AATACTAGGA AAATAATCCT CCTCTTGTCT AGGAGTTTCT GCTACTGGGA 960
GCCACAGGGT AATCAGCTCA CATGACATAC CCAGAGGCGA ATGCTAGCCT GTGCTGTTTT 1020
TGAACATACT CAAACAAAGG CTGATTATCC AAACAAGAAT TTGGACTGCA GCAGTCGGAC 1080
CAGTTAAATT ATAGTTAGTA AAACTTGGTG CCTTGTGAGC TTGGAATGTT ACAATTGCAG 1140
CTGGATCTTC GTTTGTCAGG CAGCCTTACT GCACAATAAA ACCAGAGATT TTTATCTCCG 1200
CAGGACTCAG TTTAACTCCT TGGGTGCAAA CAGAAAAGTG CCAGCTATCA TACGTCAGAA 1260
TCCTGGCAAC ATCTGTCCCC ACTCCTGTCA GAGTTCATGA GGCAGTGGCA TTTTCGTGGT 1320
GTTCTGTAGG AAAGTGGGAG GACAGGGGCA AGTTGCTCTT CTTCTTAGAT CTTATGTTGG 1380
AGATAATAAT TTTTATTTAT TCGTTACTTT AACAACATTT TTTGTTTTGA GATGGAGTCT 1440
CGCTCTGTCA CCCAGGCTGG AGTGCAGCGG TGTGATCTCA GCTCACTGCA ACCTCTGCCT 1500
CCCAGGTTCA ACCAATTGTC CTGCCTCAGC CTCCTGAATA 1540
|
