| Tag | Content |
|---|
EnhancerAtlas ID | HS146-11577 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr5:32767840-32769250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr5:32768173-32768184 | TCTTCCCGCCC | - | 6.14 | | Six3 | MA0631.1 | chr5:32767972-32767989 | AAGAGGGTATCATGAAG | + | 6.43 | | ZNF263 | MA0528.1 | chr5:32768169-32768190 | CTCCTCTTCCCGCCCTTCTCC | - | 6.06 | | ZNF263 | MA0528.1 | chr5:32768059-32768080 | CCCTCCTCTTTCCCTGCCTCC | - | 6.19 | | ZNF263 | MA0528.1 | chr5:32768062-32768083 | TCCTCTTTCCCTGCCTCCACC | - | 6.86 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_46523 | chr5:32766014-32770299 | Osteoblasts |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I032766 | chr5 | 32767018 | 32770339 |
|
Enhancer Sequence | ATAAAGCAGA AATGAAAAAA AAAAGCCATC CATATAAAAA CCTGTATTTT TGTTCATCTC 60
TTCTTTGTAA ACACATCTCT AGGTGACTCA AAAAGTTCAA GGGAAGCTGT CCGAAGTTCT 120
CAGGACAAGT TTAAGAGGGT ATCATGAAGT CAGAGAAATT AGAATTACAT GCTCCTTCTG 180
ATTTTGGACG ATCAGAAGTA ATGAGGCCAG AAATTGGGCC CCTCCTCTTT CCCTGCCTCC 240
ACCTCCGTTT GACCTGATCA CCCCTCTTCC TGTTTGTATT GCTGCCCGGC ACAGTTGCAG 300
GGTGAGTGGG ATGCCTGCTC CTGATCCTGC TCCTCTTCCC GCCCTTCTCC TGTTGGGTTT 360
TGGTTTATGC CTTTGCCTAC CTCAACTTCG TGCCTTGACA GGACACAGAC CTCAGGGAAG 420
AGAGGCCTGC ATGTGTCCCG AGCAGTCTTG TGGGGGTTGG GTCACCAGCC TTTCAGAGGC 480
ATGTCTGGCT GGCACTGGTG AATCATCAGG GCCTAGGACA AACATCACTC ACTTGGTCAT 540
CTGAAGGCCA GGAACGATTG TGTCATTATG TATGTGCATT TCTCAACTAA GCCTTCAAGA 600
GGGTGATGGG ACGAGAAGCA TCTGTATATG ACGCATGTGT GACACATCCA AAGGGCAAAT 660
ATATCATATG ACCATATTCC CTGCATGAGC CTTGGGAGAA TTTTCAAAAG TCATTCTCAC 720
TTACTTGTGC TCCATACCCA CCAATTCCAA AAACTGATGC CTACAGAGAT CTCCTTGTTG 780
CTTCCCATGA ACAAGACCAG CTTTCCTTGC TGAGGTGTGC TTATGCCTCT GGATTCCGTG 840
TGCCAGCTGT GTGACCCTCT GTTGTCCCTG TCATTACAGG AGGTGAATGA GGGCCCTAAC 900
TCTACCTAAT GATCTTCCTA AGACTGCTTT TGTTTAATGA TCCAGTCTGT TCTAGGTCAT 960
GAGAGAGAAA ACAGTCTGCA GGCAGCCACA CCTCAGGAAG GTCCAAGTTA ATTTGCCAGC 1020
CCAGTGCATT GCTACCAGTT CAGAGCTGAG TCCACGATGG GGACAGTTAT TTGGAAAACT 1080
TAGGTCAGAT CCCACCCTAA GTAAGTTCTA ACTTCAGTCG GGGGAGCAAG AAGTATGCCA 1140
GAGGGTTCAG AGATGCTTCC ACTATGCACA GAGTTGTAGA TGAAGACCCC AGCTCTCTCC 1200
CTGTGGTGCT TCCTGTCAGT CACCTGCCCT TTGCATTTTC CCAGAGTTCC ACTGGGATAA 1260
AGGCGCAGAT TTTCAGCTTA ACTTTCCTCA AGGCTAAAAT ACGTCATCAA GTGACCAAGT 1320
GAGAATTCCA TGAAGACAGG CCCACTATAG AACAGGAATT GGGGTCTCTG TCAGTAAGAA 1380
AGAGACCTCC CTCTGTTTGG TGCTGAGGAG 1410
|
