| Tag | Content |
|---|
EnhancerAtlas ID | HS148-01721 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:225654800-225655940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr1:225655275-225655286 | TGGGTGTGGCC | - | 6.62 | | ZNF263 | MA0528.1 | chr1:225655419-225655440 | AGAGGAGGATGGAGCAGAGGG | + | 6.48 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_20496 | chr1:225654279-225657087 | CD56 | | SE_25957 | chr1:225654288-225656348 | Duodenum_Smooth_Muscle | | SE_26936 | chr1:225654521-225656353 | Esophagus | | SE_54544 | chr1:225654524-225656791 | Stomach_Smooth_Muscle | | SE_61599 | chr1:225612246-225670298 | Toledo |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I225459 | chr1 | 225647457 | 225656991 |
|
Enhancer Sequence | TAATTTAATT TAATCTAGAG AAATGATGTT TGTTTCATGT TCAAATGTTC TGGAGAGGTT 60
ACACCAGTGA CAGAGGCCCT CTGAACTTAC ACACACAAAA GGCAACTCAT TAGCAGGAAG 120
ATGAGAAAGC AGAAAGCGTC TCAAGACAGG AAGCTCGGCT TGGTGTCACC CAAATGTGTC 180
TCCCCTTGAC AAATCATCTC CCATGATCTG CCGGTCCCCG GGGAGGACAG GCAAGAGGCG 240
GTGATGGGCT GTCAATGTGC ATCTCGGCGT GTGGCAGTTG ACAGGGCACC TTCATAGGTT 300
TCTTCTCTGC AACTTCACTG CCACCCCCTC AGAAACTGAG ACCCATCGGC GGCCGGCCTG 360
AGGCACCCAC AGCTGCAGAG AGCCGGGCAC ATCCAGGGCC TTGGGTGTGT CTCTCCTCCA 420
CTGTGGTGGA GGCTCCCCTC CACTGTGCCA AGCCCAGGGG GGCTGGCAGT CCCCGTGGGT 480
GTGGCCCAGA AAGACTGGCA GTGTCTGTCC CAGACCTCAG GGCCACAGTC ACCAGATAAG 540
CACCCACTGC ACTCAAGGCC TCTCTGATCA AGTCCCACGA CCAGGCTCTC CAAGTCCTGA 600
CACCGCGGAG ACCCCCAAAA GAGGAGGATG GAGCAGAGGG CAAGGCTCTC AGCTCCGCGG 660
ACTCACACCC AGCTGCAGAG GCAGGGGGAG CCGCCCTTTC TGTGGCCGGG GAAATTGAGG 720
TCACTTCCTG TCTCGCTTCC CTCTCTCTGT GCTGGCTGCA TCCTTCAGAA GGGGGGTGGG 780
TGGCTGCAGG GCAGCGCCAG GCAAGGCTGC GGAGAAGCCG GTGCTCCCTG TGTCTAGGAT 840
GAAGAACAGA GCAGGGGGCT CCTCGGCGGT GTCGCTTCAC CTCTCTTCCT GCTCCTTGAT 900
TCTCTCCACC CCCACCACCA GCCCAGGTGG AGGCTCTCGG TGATGAAGGT GCTGGCAGTG 960
AGGGGCCTGC AGAGTCCGCA TCTCTCTGCA GCTCAAGGGG CTCTCGGAGG CCACTGGGAG 1020
CTGGAGAGGG AGGAGGTCAG AGGCCTACAA TTGGTTTTCC TGCTTGGAGA AAGAACAGAT 1080
AGGAGCTTTC TAGGGCTGCG GCTCCATAAA TAGCTCTAAC TGTCCCTTCT CTCTCTTTTA 1140
|
