| Tag | Content |
|---|
EnhancerAtlas ID | HS193-08897 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr13:27542520-27543670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr13:27543122-27543137 | GGGTAATGATTAACT | + | 6.2 | | HNF1A | MA0046.2 | chr13:27543122-27543137 | GGGTAATGATTAACT | - | 6 | | HNF1B | MA0153.2 | chr13:27543123-27543136 | GGTAATGATTAAC | + | 6.01 | | HNF1B | MA0153.2 | chr13:27543123-27543136 | GGTAATGATTAAC | - | 6 | | Stat6 | MA0520.1 | chr13:27543298-27543313 | TCCTTCCTGAGAACT | + | 6.45 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_23155 | chr13:27534939-27544739 | Colon_Crypt_1 | | SE_24001 | chr13:27541050-27544070 | Colon_Crypt_2 | | SE_27831 | chr13:27540966-27545988 | Fetal_Intestine | | SE_28781 | chr13:27540921-27547129 | Fetal_Intestine_Large | | SE_47159 | chr13:27540566-27544254 | Panc1 | | SE_50194 | chr13:27534824-27547226 | Sigmoid_Colon | | SE_52911 | chr13:27540971-27544244 | Small_Intestine | | SE_56765 | chr13:27538437-27543579 | VACO_400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I026961 | chr13 | 27535141 | 27546968 |
|
Enhancer Sequence | TCAAGGATCA CCAGGACCCT TCTCCAACTT TAATTACTGA GGACTTTCCC ATGGTTAGCA 60
AGAAAGCTAG GTGATGCTGC TGGGGACAGC CATCTTGCTT CTCCAACAGA TGCAGCGAAC 120
AGCTCGGGCT TATCTCCGCT CCCGAGCAGA CACATAGTGG GAGAAAGGGG GAGAACACAT 180
GGCAAAGGGA GAACTTCAGA GCAGGATGCA TCCCTAAGCC CCAGCTGCCA GGACTGGGAC 240
CAGGAGTCCC CAAGGACTGC AGCCGTGACT CATCCAGGCC TCGGTACCCT CCCATCTCTG 300
AGGTTTTCTG CTGTGGCTCT GGGGCTCTTG TGCCCAGTGT CGCTTTGGGG CTTTCTCCTG 360
GTGGAGACTT GGGACACTCA GTGTCGGAGC CTCCCAGCAG CATGAGGAAC GGGGTGCAAA 420
CAACGCAGAC GACCCAGCTC CCCAAGAGGG GTCTGACTCC TGCATCCAGT GAGGGCTGAG 480
TCAGAGCCAA GCGGAGCCTA TCAGTGCACA ATCCAAACAC CAGCCAAGGC CCCGTGGCCA 540
GGCCAGTCAT AAACCCACGG CCACAAAAAC AGGCCAGAGA GCCCAGGAAT ACAGCCCTGC 600
CCGGGTAATG ATTAACTGGC ATCCAGGGGT CCTGGAGGTC AGAGCGATAA TGAGAAAGTT 660
TCCCTGAACT CTCTCAAGTG CAGAGGGCCT GGGGAGGGGC CCTGCTGGCG CCGATTCCTG 720
GGCAAACACT TCCTGCCCCT CTCTTTTCAA CGACCAAACA GCCTCAGCCC CTCTCACCTC 780
CTTCCTGAGA ACTGGGGAAC TGACATCACA AACGCAGGGC CTCAGGGCCC TGGTAAAATC 840
CACTGGGAAT AGCCAACGAG GGCATCTTCC CAGGAGGCTG AATTTCCTCA AACACGAGGC 900
TGATAAGCCC TTTCAAGAAG ACAGGGCTTC ATGCTTATCT TTATTGTCTG GCATGTCCTG 960
AGACATGGGA GCCACTCTGT TTGAGTGAAA CTAGAATATT ATGTTCAGCG AGACTTTCTG 1020
CTTTCTGATT TTTCTAGTGC TTTTGTATCT TGCAGTGGAA TTCTCCAGCA ACTTTCTTCT 1080
GAAATTCCCA AACAACTTCC AGTGCAGAAC TCCTGCCTCG GTTTAAGTTA AGGAGGTTTG 1140
CTAAGGCCCC 1150
|
