| Tag | Content |
|---|
EnhancerAtlas ID | HS129-01325 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:68280500-68282400 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr1:68280799-68280810 | TGTGGATTGGA | - | 6.62 | | HNF4G | MA0484.1 | chr1:68281995-68282010 | AGAGTGCAAAGGGCA | + | 6.04 | | Spz1 | MA0111.1 | chr1:68281220-68281231 | GCTGTTACCCT | - | 6.62 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_00688 | chr1:68276814-68285074 | Adipose_Nuclei | | SE_01639 | chr1:68280968-68282748 | Aorta | | SE_27870 | chr1:68277074-68285791 | Fetal_Intestine | | SE_28821 | chr1:68277189-68285946 | Fetal_Intestine_Large | | SE_52846 | chr1:68279466-68285229 | Small_Intestine | | SE_64727 | chr1:68279957-68282378 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I067811 | chr1 | 68277214 | 68285675 |
|
Enhancer Sequence | CTCTGCAGCC TTGTACAAGT TACTGAAGCT CTCTTGAGTT GTACTGTCTT CTGTAAAATG 60
AACTAATTAT ATTGCCCTAA TGGAGTTGTA ATGCCAGGTC AACAACAGAC ACACAACAAA 120
GTTACTTCCC ATAATCAAAG TTGTAAAAAG TTAGTTTCAA AACCAAGCTG CACTTTTGAG 180
ATTCCATTTT TCATTTTTAT CCAGTTTGTG GCCATTCCCA AAGGACTCCT TTCAGGTGCT 240
TCTGGAAAGT GTTACCATAC AAAAGACTTC TAGTTCTCAA GGGGGAATGG AGAAATACAT 300
GTGGATTGGA AATTCAATCC AAACAAAACC TCTCTAAAAA TTTTTTAAAT GGTATTTGTA 360
TCCAGGAAAT CAAGGCCACA AATCGTTTCT ATGAATGAGA ACTTTACAGG TTGCCTTCCC 420
TCACAATTTT TCCTTCACTT ATATCCCTGA TAAAAATAAG AAATGCTGCT GGATATAAAG 480
CAAAATTAAT GTTGACCACT AAAGCCATTT CTAGTCAAAA TTCAATAGCC TACATACACC 540
TCTTGAAAAA ACAATTTGCT CCCAGGCTCC GTATGATGAC GCTGGCCATG AGTAACACTC 600
ATGTCCCAGA ATCCTCAGAT TTAGCTTTCT CAAGAAAACT TTCCATGAAA CACGACTTGC 660
CAGGACAAGG CCTTGCGGAG GCTCCTTGTG TACCTGTGGC CCTCATCCCC AGAGTGCTGT 720
GCTGTTACCC TGTGGGTTAC TGTGTCGAAA TGGAAGCGGT GACGTTCTTC CTTCAGGGAC 780
ATTCCTTTTG TTTTTACCTA GCAGCATACA CCAATAATTT GTAAGTAGGA AGAGTTTTCT 840
GTTCATTTTT TTCTTAATGG ACAGATTTAG ACAGCCCAAA GGTAGGGCTC GGTATGTGCT 900
GCGGGGAGGG GCTCAGAGGG CCGGCATGAG GGAGGATTTG TGCCCAAAGG CTTCTCACAG 960
ACTCCGTAAC TAGATGAGGA AATGAGCCAG GATCCACAAG ACTCCTCAGC GGCCAAATCC 1020
CGAGTTCTCC TTCTGTCAAT CATCTGCACT GCAGAGACTT AGAGTACACT CCGGCAGCAA 1080
GAAGGCTGCT CTCCCAGTGC TCCTGCCTTG ACCATGCCCT GGAGTTACCT GGAAGCTTTA 1140
TTAGAGACTG TACCCTCTGG GCCCCATGCC AGGGCTGGGT GCGGCCGGGG CTCCATGATT 1200
TTCAGTCACT CCTCAGCTGA TCCTAACATG CACATAAGTT TATGAACCGC TGCCCTGGTC 1260
CCTTCTGCCT TCAGTGAGGC TGCGGAAGCT GCTAGAGCCT ATTATCTTGA GACTTTTTTT 1320
TCTTTTCTTC TAATGAAAGA AAAAGATAAT GTACGAAATC ATACATTTTG AGCTTTCCTC 1380
AAGTCAAGAA AGTTTAGGTC AGAGTCCTTA GTGTGAGTTT ATCCCTTTGC CCCACCCACC 1440
CTAATGAAGA TTACAGCCGA CCGTAGTAAC TGGAGCATAG AGCGTGCTCC TGGGCAGAGT 1500
GCAAAGGGCA CCCTTTCAAA GAAGGTGGAA GGGAAATGTA TTGGGAAGTT TATGAAGGGG 1560
AGTAAAGAAA TTTAAGAAAC AGATTCACTG CTCTTTGGAT ATGCGTGCAA GGGCTTTCAC 1620
GACTTTCCAA GCCCCTGCCT TCATCTGGAC TCCTGTTCCT CCTGGACACA CTCACCCTCC 1680
AGTCTAGTTA CAAATTATTC ACTCTTAGGA CAGGGCCCTC TGCCTCCAGC TCAAGCCAGC 1740
TGGAGACCTC TGCCCTCATC CCCACCCCAG GTTTCCAGGT GGGCCCTGCC ACTTACGGTG 1800
TGACTCCTAA ATACCTGTGG GGCAGCAGTG AGCCAGAGGG GTGGGGAAGA GTATAGATGG 1860
GGCTCTCTCC AGGACTGACT CCTGCGTACT CAGCCGTCCT 1900
|
