| Tag | Content |
|---|
EnhancerAtlas ID | HS092-11327 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:13030050-13032100 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr12:13030402-13030413 | TGTAAACAAGA | - | 6.02 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_02173 | chr12:13030262-13031253 | Aorta | | SE_23547 | chr12:13029794-13031250 | Colon_Crypt_1 | | SE_23547 | chr12:13031576-13032129 | Colon_Crypt_1 | | SE_24533 | chr12:13030302-13030703 | Colon_Crypt_2 | | SE_24533 | chr12:13030713-13031131 | Colon_Crypt_2 | | SE_28138 | chr12:13029843-13031213 | Fetal_Intestine | | SE_34394 | chr12:13029943-13032936 | HCT-116 | | SE_57272 | chr12:13029850-13031356 | VACO_400 | | SE_57272 | chr12:13031594-13032176 | VACO_400 | | SE_64427 | chr12:13030014-13031054 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I012876 | chr12 | 13029846 | 13032176 |
|
Enhancer Sequence | TAGATGCTTA ATATATAGCA CTGCACTGAA CTGAAATGAG TAGTGACACT TGCCAGACAG 60
TCTTGCAAAA GAGGAACAGG TGAATCCTTA ACACAATTCA AGGTCTTATA GGAAGAAACT 120
GCCAGTCAAC CAAAACTAAA CCGAGGCATA CATTTCTTTC CTCACCTGGC TTACAATGCT 180
GGAAGGTCTC TGGTTTCCTC TAAAGTGCCC TGGGTTTAGC CCATTAAACC TTATCTGTCT 240
TATAAACCTT GCCATGAATA TGCTTATCAG CTTCTTCCTG GGAGCATAAA ATGGGTTTGG 300
ATAATGACTA TAAAGCGCTG GAATAAGGAA GGTGCTCAAC AGAAGTTGTT AGTGTAAACA 360
AGAGCAGGTT AGAAGTGAGA AGAAGGTGCT CAGAGGACAG AGGAGATATG GGGAAGGACT 420
TGGAATTAGT GGGGTGGAAC TGGGGAGGAG AGCAGGAGGC CTGGCACTGA GAGCATCTCC 480
TTCCCAGCTT GTTCTAGACA AGAGTAGCCT TGCCTGCCAG AAGCCCTGAG ATTACAGGTG 540
AGCTGGATCC CGAGAAATGA AGTCCCTGAC TAATAGCAAA TAAAGACACG GCCATTTGAT 600
AGTTCTGTTC TACATCTCGG AATGGGTAGA AATACAATAA TAGCACCAAA CATGAATTAT 660
GGAAAACAAG CTGTGAATGG AGACATTTGC TAAGAGATGC CAGCCCGGCT CAGCGAAGTC 720
AATTCATCAG CTATTTTCAC TTGGGAAAGA GAAATTAAGG GCAGAGCCGC AGTCCCTGCC 780
AAACCTAACA GTCTAAAAAG CAGACTGTGT AACTTACCAA GGCCTCAGGG CAACATTAGC 840
TGCAAATGAG CTCAGCAGGG CGGGGGCCTC CGCACAGTTC TCTAGGGGGA GAGATGGCAG 900
GGGCCACAGC CTCTAATGTT AAAGCCACCT GCAGGGCCAG AGGGCCTCTC TGGAGGCAGA 960
GGGATGCAGC AAAGACTACT TGGCTCTGCA GTCAGGGCTG GGCCGGGTGG TGCCGCACCG 1020
CTTTCTAATG GTAACTTAAC CTCTCCAAGC TTCTTTCCTC ATCTATAAAA TGAGGCTAAT 1080
AGCATCTGCT CTGCAGAGTT TCTGTAAAGA TTAAAAACAA GACAAAGCAA GCACAAGGGC 1140
TTTGGAAACT GTAAAAGCTC TGGATATCAG ATGTCATTAT CATGAAAGAG AAACAATACT 1200
GGTTAAAAAC AAAAGTTTCC TTCTGATGAC TATTCCATGG TGTATTTTAG TGAAAGGGAA 1260
AAAAAATCCT ACTGTCTATA GATAAAATAT ATATATTTTT TCCTGCAGTA AGCAAATAGG 1320
CTTCCGATAA AAAGCTGACA TAGGGGCCAG GCACAGTGGC TCACACCTGT AACCCCAGCA 1380
CTTTGGGAGG CTGAGGGGGG AGGATCACTT GAGGTCGGGA GTTCCAGACC AGCCTGGGCA 1440
ACATGGTGAA ACCCCGTCTC TACTAAAAAT ACAAAAATTA GCCAGGTATG GTGGTGCGCG 1500
CCTGTAGTCC CAGCTACTCA GGAGGCTGAG GCAGGAGAAT TGCTTGAACC GGGAAGGCAG 1560
AGGTTGCAGT GAGCTGAGAT CATGCCATTG CACTCCAGCC TGGGGGACAG TGTGAAACTC 1620
TGTCTAAACA AACGAACAAC AAAAACAAAA ACTGACATAG GGAAATGTTT TTCCCCCTGG 1680
ATGGGCCCTG TCTTCCTCTG CCCTGTGTTG GCCTATCCCT ACCAGCCCCT TTGTGTCACC 1740
TGGAGAGGCA GCCTTTAACA TCAACAGCCA GGTGCACCTT CTAAGGCAAA CCTGGCCTAT 1800
GCTGGCAGGT ACACAGGTGA AGGGATACAG GTTCATAGTG CTTCTAACCT TTTTACTCTC 1860
TATGGATTCC TTTGAGAACG TGATGAAAGC CATGGGCATG GAAAATGCTC TCTTTTCTTC 1920
TCTTTTCTTT CTTGGGGTTG TGCCTAGGCT GGAGTGCAGT GGCATGATCA CAGCTCACTG 1980
CAGACTTGAG CTCCCAGGCT CAGGTGGTCC TCCCGCCTCA GTCTTGGGAG TAGCTGGAAC 2040
CACAGGTATG 2050
|
