| Tag | Content |
|---|
EnhancerAtlas ID | HS007-17412 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr9:100907660-100909760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr9:100907997-100908009 | GTTTGTTTGTTT | + | 6.32 | | Klf1 | MA0493.1 | chr9:100908994-100909005 | GGCCACACCCA | + | 6.62 | | LMX1B | MA0703.2 | chr9:100908826-100908837 | TTAATTAAATC | - | 6.02 | | PBX1 | MA0070.1 | chr9:100909411-100909423 | ACATCAATCAAA | + | 6.74 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_09950 | chr9:100906687-100909717 | CD14 | | SE_24386 | chr9:100906486-100908048 | Colon_Crypt_2 | | SE_24386 | chr9:100908125-100909316 | Colon_Crypt_2 | | SE_26852 | chr9:100904207-100909935 | Esophagus | | SE_27659 | chr9:100903802-100910551 | Fetal_Intestine | | SE_28584 | chr9:100903818-100910565 | Fetal_Intestine_Large | | SE_42027 | chr9:100906616-100908027 | LNCaP | | SE_42027 | chr9:100908189-100909398 | LNCaP | | SE_53152 | chr9:100904184-100910435 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I098141 | chr9 | 100904020 | 100910418 |
|
Enhancer Sequence | GCAGGCCAAC TCCTTGGATA TTTGAAGACA GAGGACCCAT TCCTTGAGTA TGTTCTTGTC 60
CAGGATGAAC AAACCCCTAG AACTGGAAGA GACTTCCAAA ATGCCAGACT AGCCCATACC 120
CTGCCTTTCT AGAAGGGCAA TTTGTATGGA GGGAACAGAT ATGTGCTATG GAAGGCTCTG 180
AGGTTCCAAA CAGTTGGCTA GGACAGGGCA TAGAGGGCTT TGATGAGAGA GGCAGAACAT 240
TATCTGCAGG CAGCAAGGAG TCCTGGGAGG CATCTGAGCA GCGGAGTGAT GTGGACACAC 300
ATCGGCTTGA GAAGGGTCAG GTTGGCCTTG GTTTTTTGTT TGTTTGTTTT TTGAGACAGA 360
GTATTGCTCT GTCGCCCAGG CTGGAGTGCA ATGGTGCGAT CTTGGTTTAC TGCAACCTCT 420
GTCTCCCGGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ACTACAGGCA 480
TGTGCCACCA CGCCCAGCTG ATTTTTTATT TTTGGTAGAG ACAGGGTTTT GGTATGTTGG 540
CCAGGCTAGT CTCGAATGCC TGACCTCAAG TGATCTCCTG CCTTGGCCTC CCAAAGTGCC 600
AGGATTACAG GTGTGAGCCA CCATGCTGGC TAAGGCTGGC CTTTAAGATC ATGGCAGTGA 660
AATGCTCCTC TCCACTCTCC CAGGCACCTG AAAGCCACGG TGTCCATTAG GCCCTCAGGC 720
CCATGTCCCC TCTGGCCTGT CTACTCCCAG CAGGGTTCCA GGGCTGACCC CCAGGGGCTC 780
TGCCTGCCCT TGCTTTCATT CCTCCCCACC CTCCACACCT CACAGCAAAG TCCACCTTCT 840
TCACCCCCTC CCTGGAGTGA CTCTGTGGCA GGCTGGGCCC CAGGCTCAGG AGCACAGTCC 900
TGGCCTCTCC CCAGCCTTCC CCTGCTGCCT TTGTTCCCTG AGTACAGTCC CTGGTTGCCA 960
AGGCTGCAGG TTGCGAAACT CACCTCCAGC CTCCCTCTAA CCAGCTCACC CTGGGTCACA 1020
ACAGGCAAGA GGGAGGGACC CTGCCTGCAG TGTCACTCCC TTTGGGACAT CTGAAACTGC 1080
CTGGGGCAGC CCGGCCCCTC TGAGAAGGAC TTCCTGCACG CTGTGGCAAG GCCAGACATC 1140
TCCCAATCTC AATGCAATTT ATGTACTTAA TTAAATCATT AGCTAGCTTG TCCCTTCCTT 1200
GTTCTCACAT CACTCACCTA CTGATACATC TCTGTGCCTG GCACAGAACG TAATCCTGGT 1260
AACAAGTAGG AGCTGATGCA AATCAGTGCC AAACCTCAGG GGCCTCATGT CAGTGAAGTG 1320
AGAGCAAGGC CCGAGGCCAC ACCCAGGTCT GGGCTCCCAT TCGGGTCCTG GACACACTGC 1380
ACAGGGTCCT CTGGGAAGTC ATCTTCCTGA GCCTCAGCGA CCTCATCTGT GCAATGGGGC 1440
AAGATCCCCT ATAAATGGGG CTAATGTTCA TAAGGTATCA GCATAATCAC TCCAACCCTG 1500
GTTACAACAT AATAAAGAGC CTCTAAGGCC TGTCTGTGCA GGTAAGTGCT ATGGCATGGT 1560
GCCTGCACAG TAGTAATGGA TGTGGTTACT TAATAAGAAA CATATTGGCC AGGTGTGGTG 1620
GCTCATGCCT GTTATCCCAG CACTTTGGGG GGCTGAGGCA GGAGGATCCC TTGAGCCCAA 1680
GAGTTTGAGA CCAGCCTGGG CAACATAGTG AGACCCCATC TCTACTTACA ATAAGAAAAA 1740
ATTAAAAAGA AACATCAATC AAATGCAAGA TGTGGACCCC ATCTGGACTT TGAGGCAAAC 1800
AAACCACAAG CAAAGTGGCA TGTATGAGGC AACCAGGGAC CATTAACATG AATTAGGAAT 1860
CAGGTGACAC AAGAGTTATT ATTAATGTGA TCCTGGCATT ATGGTTATGT CAGAAAATGT 1920
CCCTGGTTTT AGAATTGCAT ACTGACATGT GGTAGGGGGC GGGGGGCAGA GGTTGAAATG 1980
ACAAAATGTC TAGGATTTGC TTTAAAATAC TTCAGGTAAA AGGGATGAGT GAAGCAAGAG 2040
GGCAAACTTG ATAATTCTAG AATCTGGGCT GAGGAAAGTT CATCATATTA TTTTTATCTA 2100
|
