| Tag | Content |
|---|
EnhancerAtlas ID | HS118-19390 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr9:100907710-100909650 |
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 | TGTTCTTGTC CAGGATGAAC AAACCCCTAG AACTGGAAGA GACTTCCAAA ATGCCAGACT 60
AGCCCATACC CTGCCTTTCT AGAAGGGCAA TTTGTATGGA GGGAACAGAT ATGTGCTATG 120
GAAGGCTCTG AGGTTCCAAA CAGTTGGCTA GGACAGGGCA TAGAGGGCTT TGATGAGAGA 180
GGCAGAACAT TATCTGCAGG CAGCAAGGAG TCCTGGGAGG CATCTGAGCA GCGGAGTGAT 240
GTGGACACAC ATCGGCTTGA GAAGGGTCAG GTTGGCCTTG GTTTTTTGTT TGTTTGTTTT 300
TTGAGACAGA GTATTGCTCT GTCGCCCAGG CTGGAGTGCA ATGGTGCGAT CTTGGTTTAC 360
TGCAACCTCT GTCTCCCGGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG 420
ACTACAGGCA TGTGCCACCA CGCCCAGCTG ATTTTTTATT TTTGGTAGAG ACAGGGTTTT 480
GGTATGTTGG CCAGGCTAGT CTCGAATGCC TGACCTCAAG TGATCTCCTG CCTTGGCCTC 540
CCAAAGTGCC AGGATTACAG GTGTGAGCCA CCATGCTGGC TAAGGCTGGC CTTTAAGATC 600
ATGGCAGTGA AATGCTCCTC TCCACTCTCC CAGGCACCTG AAAGCCACGG TGTCCATTAG 660
GCCCTCAGGC CCATGTCCCC TCTGGCCTGT CTACTCCCAG CAGGGTTCCA GGGCTGACCC 720
CCAGGGGCTC TGCCTGCCCT TGCTTTCATT CCTCCCCACC CTCCACACCT CACAGCAAAG 780
TCCACCTTCT TCACCCCCTC CCTGGAGTGA CTCTGTGGCA GGCTGGGCCC CAGGCTCAGG 840
AGCACAGTCC TGGCCTCTCC CCAGCCTTCC CCTGCTGCCT TTGTTCCCTG AGTACAGTCC 900
CTGGTTGCCA AGGCTGCAGG TTGCGAAACT CACCTCCAGC CTCCCTCTAA CCAGCTCACC 960
CTGGGTCACA ACAGGCAAGA GGGAGGGACC CTGCCTGCAG TGTCACTCCC TTTGGGACAT 1020
CTGAAACTGC CTGGGGCAGC CCGGCCCCTC TGAGAAGGAC TTCCTGCACG CTGTGGCAAG 1080
GCCAGACATC TCCCAATCTC AATGCAATTT ATGTACTTAA TTAAATCATT AGCTAGCTTG 1140
TCCCTTCCTT GTTCTCACAT CACTCACCTA CTGATACATC TCTGTGCCTG GCACAGAACG 1200
TAATCCTGGT AACAAGTAGG AGCTGATGCA AATCAGTGCC AAACCTCAGG GGCCTCATGT 1260
CAGTGAAGTG AGAGCAAGGC CCGAGGCCAC ACCCAGGTCT GGGCTCCCAT TCGGGTCCTG 1320
GACACACTGC ACAGGGTCCT CTGGGAAGTC ATCTTCCTGA GCCTCAGCGA CCTCATCTGT 1380
GCAATGGGGC AAGATCCCCT ATAAATGGGG CTAATGTTCA TAAGGTATCA GCATAATCAC 1440
TCCAACCCTG GTTACAACAT AATAAAGAGC CTCTAAGGCC TGTCTGTGCA GGTAAGTGCT 1500
ATGGCATGGT GCCTGCACAG TAGTAATGGA TGTGGTTACT TAATAAGAAA CATATTGGCC 1560
AGGTGTGGTG GCTCATGCCT GTTATCCCAG CACTTTGGGG GGCTGAGGCA GGAGGATCCC 1620
TTGAGCCCAA GAGTTTGAGA CCAGCCTGGG CAACATAGTG AGACCCCATC TCTACTTACA 1680
ATAAGAAAAA ATTAAAAAGA AACATCAATC AAATGCAAGA TGTGGACCCC ATCTGGACTT 1740
TGAGGCAAAC AAACCACAAG CAAAGTGGCA TGTATGAGGC AACCAGGGAC CATTAACATG 1800
AATTAGGAAT CAGGTGACAC AAGAGTTATT ATTAATGTGA TCCTGGCATT ATGGTTATGT 1860
CAGAAAATGT CCCTGGTTTT AGAATTGCAT ACTGACATGT GGTAGGGGGC GGGGGGCAGA 1920
GGTTGAAATG ACAAAATGTC 1940
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