| Tag | Content |
|---|
EnhancerAtlas ID | HS053-00488 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:17846070-17847550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:17846103-17846124 | AAAAAGAAAATGAAAAAAAAG | - | 6.44 | | NFIA | MA0670.1 | chr1:17846572-17846582 | ACTTGGCACC | - | 6.02 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_23081 | chr1:17846244-17847819 | Colon_Crypt_1 | | SE_23747 | chr1:17846263-17847734 | Colon_Crypt_2 | | SE_24767 | chr1:17846187-17847680 | Colon_Crypt_3 | | SE_26573 | chr1:17846174-17847852 | Esophagus | | SE_31687 | chr1:17846175-17847707 | Gastric | | SE_34117 | chr1:17846177-17846721 | HCC1954 | | SE_34117 | chr1:17846737-17847596 | HCC1954 | | SE_50079 | chr1:17845934-17847790 | Sigmoid_Colon | | SE_52601 | chr1:17846233-17847203 | Small_Intestine | | SE_57435 | chr1:17846774-17847458 | VACO_503 | | SE_68684 | chr1:17846257-17847905 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I017519 | chr1 | 17846138 | 17847663 |
|
Enhancer Sequence | GCCACTGTGT GACAGAGAGA GCCCTTGCCT CAAAAAAAGA AAATGAAAAA AAAGGAGGAA 60
ACTCCATCAT GGCCAACCTG GTGAAACCCC ATCTCTGCTA AAATACAAAA ATTAGCTGGG 120
CATGGTGGTG GGTGCCTGTA ATCCCAGCTA CTCGGGAGGC TGAGGCAGGA GAATCACTTG 180
AACCTGGGAG GTGGAGGTTG CAGCGATGCA GTGAGTCAAG ATCGCACCAT TTTACTCCAG 240
CCTGGGCGAT GACCAGAGAC TCCATCTCAA AAAAAAAAAA GAGGAAACTG AGGCTCAGAG 300
AGACAAGGCC GGTTGCATGA TGTCACATGG CTGGAGAGGG CGGGGATTGG CACTTGGATC 360
TTTCTGACTT CAAAGCATAT TCCTTTCCAC CTTCTCTGGC TAAAAGGGGT GCAGCCCATG 420
GGTGACCCTC CAACCCTGCC CTGTACCCAG GCCCTGTGTG CCTTCCCAGG CCAGCGGGCA 480
GTGGTCGGAG CTCAGCCCTA CTACTTGGCA CCCCCCTCTG GATTCCCCAT CTTGGTTCTT 540
GCCCCTCCCT TCCTCACCCA GGCCAGCTTC CTGGTCCTCC CAGGCTGGTT GATGGATGGC 600
TCAGCCCCGG CTGGCTTGAC TCAGTCTAGC TTTTCCTCGT GGACTGCCAG GGCTGCCTCC 660
TGTCCTCCTG CTTACCGCCC TTGCCCGCCC AGCAGGTCGG GCAAGTGAGT GACTCACACA 720
CCTGGGCTCT GTGTGGGCCC AGCCCGGGGA GCCAGCGTAC TCACCCTCTG GGCTCCTGCC 780
TGCTACTTCA ACTGACAGAC GGGACCCTTC CCAGTAGAAG GGGGCTGCCC CTGTCACTTG 840
TGCTCCCTTC CCGGAGGACT GCGATTGGAC TGCACAGGAT TGAGGTCAGT TTCCTTTCTC 900
TTTTTAACCA TCTCTGCCCC TCGCTAAATT GGAGGAGAAT CTTTTGGAGG TCGTGGGGGA 960
GGGGTCTCAG CTGTCATTGA CACCCTTGTG TGTCAGGCCC TGGGGCACCC TACTCCCTCC 1020
CAGCAGGTGC TGGAGCTTGG GGACACCTTG GGATGGACTC TGTGAGGAGA ACCGTGCTGG 1080
GTGCCTCTAT GGGTGTGACC CCGATCCTAC AGCCACCTAG CAGGGCAGGT CACGGCAACC 1140
TGGAGTGAGA ACGGCAGAGG TGGACTGCAA GGGCGTGTGT AGGGGGGACT TCCCTCACTT 1200
CCTTCTTAGG GTCACAGAGT GAGGGATGCA GCTTGAGATG GCTTCAGTTC AATGGCATCA 1260
TTTTACAGCT GGGAAAACTG AGGCTTGGAG GAGAGGGAGT AACTGAGGTG GATTGATGCA 1320
TTGGTGCTGG AACTGGGGTT GGAAGGCGGA CTGGCTGACT CCCCGCCCAG GGCTCCTTCC 1380
TTGGTCCTCC ATGCCTGTTC CAGGCTGTTT CCCCCTGCTT TTCCACTCGG CTCTCTCCCA 1440
TGCCATCCGG GCCTCAGCAG GGAGGAGGAA TGCAGCTGGT 1480
|
