| Tag | Content |
|---|
EnhancerAtlas ID | HS034-08956 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr14:55543710-55544900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr14:55544335-55544346 | CCACACCCTGT | + | 6.14 | | KLF5 | MA0599.1 | chr14:55544092-55544102 | GCCCCGCCCC | + | 6.02 | | SOX10 | MA0442.2 | chr14:55544052-55544063 | TGCTTTGTTTT | - | 6.02 | | SP1 | MA0079.4 | chr14:55544089-55544104 | TAAGCCCCGCCCCTT | + | 6.51 | | SP2 | MA0516.2 | chr14:55544088-55544105 | ATAAGCCCCGCCCCTTA | + | 7.61 | | SP4 | MA0685.1 | chr14:55544089-55544106 | TAAGCCCCGCCCCTTAC | + | 6.64 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_24786 | chr14:55543633-55544989 | Colon_Crypt_3 | | SE_26711 | chr14:55543542-55545313 | Esophagus | | SE_27630 | chr14:55543381-55545303 | Fetal_Intestine | | SE_28543 | chr14:55543226-55546173 | Fetal_Intestine_Large | | SE_36360 | chr14:55540252-55546494 | HMEC | | SE_64650 | chr14:55543220-55545298 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I055070 | chr14 | 55537320 | 55545907 |
|
Enhancer Sequence | GCAACAAAAA TGAAACTCCA CACAAAAAAA TAAAAAATAA AATAAAATGA GGATTACACT 60
CATGCCTAAC TCCACAGGGT TACGAGAATT AAATGAAGTC ATCCATGTGA AGCAGTTGGC 120
ACCTGACATC AGATGTGAGC TTATCATGGG AGCTGAAAGG CATTTTTCTA GGTATTGGGC 180
CTACAAGAGT GTTACAGTTT AGCAGAAGAA ACAGAAAAAT AGGCAGGTGT GATGTTACTG 240
ATGCAGGAGG CACGGATTGC TCTGAGTACA CCCGAGGAGC ACCTAATAGT GAAACAGCTA 300
CCATTTGTTG AACACTAGTG ATGTCTCAGA CAGTCACCCA CATGCTTTGT TTTCTGTTTT 360
CTCCCTTAGC AATGCCCTAT AAGCCCCGCC CCTTACCCAA GGCCTTTACT CACACTCACT 420
GTGTCCTCAC AACAACATAA GCAAGGGGTA AAAATTCACA GCCTGTGGAG TGCAGAGCCA 480
TGCTCTTTCC CCTTTATCAC GCAGGGCACC ATTAATATTT TAAGGCACTT CAGAAAAAGA 540
CCTGTCTCGG AGAAAGAGAG TCCAAAAGAA CATCTGTCTC CTCACCTCAC GCTACTTTGC 600
ACCTGGCCAT ATTTCCAAAT CAATTCCACA CCCTGTTTGA AAGCAGCTCA CCTTGGGGAT 660
GGATTAGAAA AATCGCAAGC CCCAGGCCTG GGTATGTGAG TGAGTTTCGG CAACAGATGA 720
AGGGCAGGCA GGCGCCCCGT CTGGGGAGGA AGTCCAGTGT CACAATTGTA CCTCTGAGTA 780
GCTGTGTTCC CAACATTCCA GAGAACAGCT CCACCCTGGA ACAGCTTTCA TGAGTTATCC 840
GCACTGACGT CAGCCACATA CCTGTGAACA CGACTTGCTT CTTGGCTGCC CACAGCTGCA 900
CTATTCCTTC TTGCTGGGTT TTGGGAGTAC ACATGAGCTA TTCATTACAG AGTTTCAGGC 960
CCACTAGCAA CTCTGAATAC CTCATATTCT AAAAGAGCAC GGCTTTTCCC AGCTCATTTG 1020
GGATTACATG AGAGATTAGC CTGTGTCCAC GAAGGCCAAC AACTACTCTG ACTGGGGAAT 1080
CGGCAAGAGA AGGCTTCCTG GAATGAGTCT CGAGGGATTT GAGCTTTGGA CAAAGGAGTT 1140
GATAAGATTT TGTCCTAGGA CAAAGAAAGA TAGAACAGGC CTAAGATAAA 1190
|
