Tag | Content |
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EnhancerAtlas ID | HS141-11277 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr2:232247920-232249060 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr2:232248534-232248545 | AAACCACAAAC | - | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_20161 | chr2:232247433-232249475 | CD56 | SE_23390 | chr2:232247889-232249113 | Colon_Crypt_1 | SE_25225 | chr2:232247694-232249271 | Colon_Crypt_3 | SE_28347 | chr2:232248078-232249276 | Fetal_Intestine | SE_47359 | chr2:232247667-232249101 | Panc1 | SE_61603 | chr2:232242399-232297770 | Toledo |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I231381 | chr2 | 232246252 | 232249475 |
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Enhancer Sequence | GAAGGAAGAC CAGGGCCAGG CAGCGGGCTG GGAGTCGGGG GTGTGGGAGC CAAGACGGGG 60 ATTGGACTAG GGCCAGGGAG GGCCCTGAAG GTAGGTGCTA AGCTGAGGTG TGTGAGGGAC 120 CCTCTGGGAG GTCTTGACCC CATGGGATGC GGAGTTGGGT TTTCCTAGCC CTGGCTCCTG 180 CCTCCGTCCC CCTGGCCTAC AGCCCCTGCA TGCCTTGGTC CCTGCCTGCT CCTCCCAATG 240 CCACCGCATG CCACCTTTAG GCTCTTGTGG GACCTCAACT CCTCAGCTTC CTGCCCCTCT 300 CCACCTCCAG CTCTCAGACC TTTCCCCTCC CTGTCACTGA ACACACTGTG AGGCCCTTGC 360 TTTGAGAGGG CAGGGAGGGC CTGGGACTGT TCCCACGGTG TCCTGTCGGG GCCAGGCACA 420 AGCTCAAACT TAAATGTGCA TATGGGTCAC TGGGCAGGGC TCGCGGGCCT GAGAGCTTGC 480 ACTCTAAGGA GCCCAGGTGC TGTCGATGTT GCTCAGCTTC TGGTCGCAAT GCAAGGGTCC 540 CTTCCTGAGC TCACCACACG CTGGGGTCAC TCCGGGCTGT GGCTACCACT GGGCCTCGCT 600 TCTGCCTTCT GCAAAAACCA CAAACTCCCC AGGGCAGCAC ATGTGTCACA GACGTCTTTT 660 TAACAGCTTT ATTGAGGTAT AATTGACAAC AGTCAACTCT ATGTGTTTAA AGTATACAAT 720 GTGGTGAATT TTGACGTGTG TAAACAACCA TAAAATCATC GCCATAATCA AGATCGACAC 780 AGTCAACGTC ACTCCCAACA GTTTCCTCTG GGCCCCTTGT AATTCCTCCC ACCTCACCCC 840 ATGTTTAGGC AATTGACATT TCTTGTCATG ATAGATTAGT TTGCACTTTC TAGAATTTTA 900 TACATACAAG GTAAGGCAAG ATAGGTGGGT GGGGACAGGC AGGCGCTGCA ATGCCTTGGC 960 TGAGGTTCAT ACCCCACCCA GGGGGCTCTG GCCTGGCAGC CCTGTCTCCA CACCCAAGAC 1020 CCTGCAGCAC GCTGCCCTGG CCCTGCCCCT GCCCCTGCCC CTCTGCCCTC ACCCACAGTG 1080 AAGACACCTC ATCACACAAG ATATATTCTT TTTTTGACTG GCTTCTTTCA TTCAGAATAA 1140
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