| Tag | Content |
|---|
EnhancerAtlas ID | HS184-10748 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr14:100602310-100603910 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr14:100603718-100603735 | AGGGTCAACCTGACCTA | - | 6.15 | | ESR1 | MA0112.3 | chr14:100603718-100603735 | AGGGTCAACCTGACCTA | + | 6.83 | | ESR2 | MA0258.2 | chr14:100603719-100603734 | GGGTCAACCTGACCT | - | 6.67 | | Nkx3-2 | MA0122.3 | chr14:100603456-100603469 | AATACCACTTAAA | + | 6.22 | | PPARG | MA0066.1 | chr14:100603716-100603736 | TCAGGGTCAACCTGACCTAG | - | 6.26 | | RREB1 | MA0073.1 | chr14:100603832-100603852 | CCTGTTGGGGTGTTTAGGGG | - | 6.15 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_17314 | chr14:100602006-100603707 | CD4p_CD25-_CD45RAp_Naive | | SE_31785 | chr14:100602826-100606275 | Gastric |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I100135 | chr14 | 100602007 | 100606275 |
|
Enhancer Sequence | AGGGCGCCCC CCGCTGACCC CAGTGAGGCA TGAGGTCTCA GAGTGGGAGG GGGGACCCTT 60
CGGACAGGAC CCTCTGATCC AGCCTCTTTA GTATGCCTGA GCAGAGGGCC AGGCCACAGG 120
GAAGCCCATT TCTTATGGGT CCCCCAGAGC CTCCCCCAGG AGCCCATGTG GGAGCACAGG 180
AAGTGCTAGA GCAGAGCCAC TGTGATGGGT CCCCAGGGTG ACCTGCGTGT CACCTTCCCA 240
CCAGGACCCT GAGTCCCGCA CGAGAGAAGG CACTTGCCTG ACGGCACATA TTCAGGGTGG 300
GAGTTTGTGT CCAGGGCTCC TGAGGCAGGC TGGGGCCAGT GCTCTTAAGA GGTATCAGTG 360
TCAGGACTCA TGTCTCCCAG TGAAACGCCA GCTGATGACC GACATTACAG AGATGGCAGT 420
AGATCTCGCT CCACCCAAAA CGCAGCCCCT TCCCTGGCTC AGGTTTCTCT CTGTCTAAGC 480
TGTGGCAGAT GGGAGGTAGT TAGGAGAGTA TGATGAGGCT TCGCAGGGGA GGAAGACCCC 540
AGGGTTGGTT GTTCATTCGA CAAACATCTT TGCAGCACCT GCTCTGTGCC AGGCCTGTGC 600
TCATGAGCAC AGCGAGGAGA GACAGGGGCA TCAGGCTGCC CTAGCTGGGC AGAGGAGGCT 660
CTTGCCAGCT GTTCGCGTGT GTCTCTGGGG CATGCTCAGG TTGGGTGTCG CCTCCCTGTG 720
AAACTGCACG CCATGTCCTC TCCTCCTAAG ATTTTTGCCT GGTGTCTTGA TTTGCCAGGA 780
TGCATAGGTT CCTGGCTGAT GAACGTGATC AATACCCCTG CCCTGTTTGC TTCTTCCAAC 840
AGCCCAGTGA GTGGGCTACG TGGTTCCCAT CTGTGTGCAA AGTGGTTTGC TCAAGGCCAC 900
ACACCTGGGA CATGTCTGTA GCCCCAGGTC TAGTGCCTGC AGGCCCAGCG CCTGTCCCAG 960
AAGGTGGCTT TGAGGAAAAC TGCCTCAATC CCACCGTTGG TCCGCAGGGT GCCAAGGCTT 1020
AGCTCTGGGC CAGGCAGCTG CCCCACTACC CCCTAGAGAT TTTGTCTTCT GCCTCTGCTT 1080
GTCCTGCACA GTCAACGAAT TCAAGTTAAT GCAACAAATC TTTTGGAGTA GAACAAAATA 1140
TAATCCAATA CCACTTAAAA AAGACAAGCC AGCCAGAATG GGACAGAGCC AGGCGCAGCA 1200
TGGGAGGCAG ACTAAGGAGC CCCTCAGTAG CAGGTGCCGG GCCGAGGGGC CTGGCCGCCA 1260
CACCACACGT GGGAGCAAGG CTGTGCTGGG ATGTCCGGGG AGGTCGTGCT TGCTCGCCCT 1320
GTGGCTCTAG TCACTGGGTC CCTTACCAGC AGGCTCACAT TCCAGAGAGA CCTGGCACAG 1380
TGAAGGGCTC AGAACCAGAT CACAGGTCAG GGTCAACCTG ACCTAGGCCA TGGGGGACTG 1440
AGAACAAGGT GCCAGGTTTT GGCTTAACTC AATCAGACCT TCCTGCCACG GGGCTCTGCA 1500
CCCTTGGCAT GGGTGAGGGC TTCCTGTTGG GGTGTTTAGG GGATTGGGGT GGCTACTGAG 1560
TCCCTTCACC TGTGAGGTTC TTCATCCATG AAATGAACTG 1600
|
