| Tag | Content |
|---|
EnhancerAtlas ID | HS095-31380 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr9:110266420-110268000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr9:110267052-110267073 | AAGGGAGAAGGGGAGGGAGGG | + | 6.38 | | ZNF263 | MA0528.1 | chr9:110267055-110267076 | GGAGAAGGGGAGGGAGGGGGA | + | 8.01 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_23179 | chr9:110266233-110267128 | Colon_Crypt_1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I107503 | chr9 | 110266177 | 110267869 |
|
Enhancer Sequence | TAAGCCTGGC TACTTTCAAA AAGTTTTTTG TAGAGATGGG GTCTCGCAGT GTTGCTCAGG 60
CTGGTCTCAA ACTCCTGGCC TCAAGCAATC CTTCTACCTC AGCCTCCCAA AGTGCTGAGA 120
TCACAGGCGT GATTCACTGT GCCTGGCCTA AAGTTTATTA ATTCTATCAC ACAGAGGAGG 180
AAATGAAAGA ACTGGAGATG AAATTGATCA AATTAGTAAT CTCCAGCCAG TCCTGAGGAG 240
ATTTAGCACT GGGCAGTGTT CGAGTTGGAT TTAAGAAGAG GCAGAGTGGT ACCACCAGTT 300
TGCCCCACGT GGGTAAGGGA GAGATTTTCT GGCAAGACTG AAGACATTCT GATACCCTCC 360
TCTCCCCTAA CATACACTTA CTCAGGTGTA AGAGTAATTC AGGCATAAGA GTCAGCAAAA 420
ACACTTTCTC AAGACGCTGT CTAGCTGTCT CAGGATCTTG TCCTGCTCAG GGTTGAGCAC 480
AAGGAGAACA CAATCCTTGC TGGCCGGGCC CTGTTCTGGA ATGACTGAGC TGTCCAGCAT 540
GGCCAGTGTG TAAATGTCAA GTAAACACCA AATTCAAGTG CAATCTAACT ATTGTGCTGG 600
GACTGTTTGT TTTAGATATA ATAGTCAGCA GGAAGGGAGA AGGGGAGGGA GGGGGAAAGT 660
ATATATCACT TCACAAGGCA AAATTATGAC TATCGTGAGC CCTCCCTTGG TCAACTTGAA 720
TGTCAAGAAA CCAATATCAA ATAAATAAAG AGCCTGCACT CCATGCTGCA AAAATAAGCA 780
TGTCCATTTG CTTGAAAAAA AGATTTTTTC AGATGAGGGA ACATTTTCCA GTCAATCACC 840
CTGCAGCAAA GTCATCCTGT TGAATTTGTG ACTCACAGCC TCTCTGTGTC AATAGACAGA 900
GTCAGCCCAG AGTTATGACT TCACAGAAAG ATGAAGCAAA AGCTGGGAGA CGAGGCAGGA 960
CCAGCTTTAA AAGAAGGCTG TAAGCTCAGA CAACAAGTAG CAAAAGAAAC ACTGACCACT 1020
CACAGGCTGG GTAATTGCAT TCGTTGCTTC TTTTTATTTC TTGCTCGTCT CCTAGAAAAG 1080
AACAACTCTG ACTTTGACTT CATCCTTTCA TTGCATTAAC ATTGACGGGG GACATGGTCA 1140
TTGTCAGGGC TATGACTTTG CCTGGTGCTC CATATACATT GTTATCTCAT TCTGTTCTCA 1200
TAGCAATTCT ATAAGGTAGG TGGTATTTGT ATTATTTTAT TTTATTTCCT TTTTTTTGGA 1260
GATGGAGTCT TGCTCTGTTG CCCAGGCTGG AGTGCAATGG CGCAATCTCA GCTCACTGTG 1320
CGAACTCTAC ATCCTGGGTT CAAGCGATTC TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC 1380
TACAGGTGCA TGCTGCCACA CCTGGCTAAG TTTTTGTGTT TTAGTAGAGA CGGACGGGGT 1440
TTCACCGTGT TGCTCAGGCT GGTCTCAAAC TCCTGAGCTC AGACAATCCG CCCACCTCGG 1500
CCTCCCAAAG TGCTGGGATG ACAGGCAGGA GCCGTTGCGC CTGGACTTTA TTTACTTTTA 1560
TTTATTATTT ATTTTATTTT 1580
|
