| Tag | Content |
|---|
EnhancerAtlas ID | HS145-26677 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr9:100908260-100909480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| 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: 7 | ID | Coordinate | Tissue/cell |
| SE_09950 | chr9:100906687-100909717 | CD14 | | 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 | chr9:100908189-100909398 | LNCaP | | SE_53152 | chr9:100904184-100910435 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I098141 | chr9 | 100904020 | 100910418 |
|
Enhancer Sequence | AGGATTACAG GTGTGAGCCA CCATGCTGGC TAAGGCTGGC CTTTAAGATC ATGGCAGTGA 60
AATGCTCCTC TCCACTCTCC CAGGCACCTG AAAGCCACGG TGTCCATTAG GCCCTCAGGC 120
CCATGTCCCC TCTGGCCTGT CTACTCCCAG CAGGGTTCCA GGGCTGACCC CCAGGGGCTC 180
TGCCTGCCCT TGCTTTCATT CCTCCCCACC CTCCACACCT CACAGCAAAG TCCACCTTCT 240
TCACCCCCTC CCTGGAGTGA CTCTGTGGCA GGCTGGGCCC CAGGCTCAGG AGCACAGTCC 300
TGGCCTCTCC CCAGCCTTCC CCTGCTGCCT TTGTTCCCTG AGTACAGTCC CTGGTTGCCA 360
AGGCTGCAGG TTGCGAAACT CACCTCCAGC CTCCCTCTAA CCAGCTCACC CTGGGTCACA 420
ACAGGCAAGA GGGAGGGACC CTGCCTGCAG TGTCACTCCC TTTGGGACAT CTGAAACTGC 480
CTGGGGCAGC CCGGCCCCTC TGAGAAGGAC TTCCTGCACG CTGTGGCAAG GCCAGACATC 540
TCCCAATCTC AATGCAATTT ATGTACTTAA TTAAATCATT AGCTAGCTTG TCCCTTCCTT 600
GTTCTCACAT CACTCACCTA CTGATACATC TCTGTGCCTG GCACAGAACG TAATCCTGGT 660
AACAAGTAGG AGCTGATGCA AATCAGTGCC AAACCTCAGG GGCCTCATGT CAGTGAAGTG 720
AGAGCAAGGC CCGAGGCCAC ACCCAGGTCT GGGCTCCCAT TCGGGTCCTG GACACACTGC 780
ACAGGGTCCT CTGGGAAGTC ATCTTCCTGA GCCTCAGCGA CCTCATCTGT GCAATGGGGC 840
AAGATCCCCT ATAAATGGGG CTAATGTTCA TAAGGTATCA GCATAATCAC TCCAACCCTG 900
GTTACAACAT AATAAAGAGC CTCTAAGGCC TGTCTGTGCA GGTAAGTGCT ATGGCATGGT 960
GCCTGCACAG TAGTAATGGA TGTGGTTACT TAATAAGAAA CATATTGGCC AGGTGTGGTG 1020
GCTCATGCCT GTTATCCCAG CACTTTGGGG GGCTGAGGCA GGAGGATCCC TTGAGCCCAA 1080
GAGTTTGAGA CCAGCCTGGG CAACATAGTG AGACCCCATC TCTACTTACA ATAAGAAAAA 1140
ATTAAAAAGA AACATCAATC AAATGCAAGA TGTGGACCCC ATCTGGACTT TGAGGCAAAC 1200
AAACCACAAG CAAAGTGGCA 1220
|
