| Tag | Content |
|---|
EnhancerAtlas ID | HS138-03757 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:226997360-226998610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr1:226998293-226998304 | AATGACCTTGA | - | 6.32 | | Esrra | MA0592.2 | chr1:226998294-226998305 | ATGACCTTGAC | - | 6.32 | | Esrrg | MA0643.1 | chr1:226998294-226998304 | ATGACCTTGA | - | 6.02 | | KLF14 | MA0740.1 | chr1:226997419-226997433 | CAGTGGGCGTGGCA | - | 6.28 | | SP3 | MA0746.2 | chr1:226997420-226997433 | AGTGGGCGTGGCA | - | 6.71 | | SP8 | MA0747.1 | chr1:226997420-226997432 | AGTGGGCGTGGC | - | 7.22 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_54921 | chr1:226997402-226998323 | Stomach_Smooth_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 226997737 | 226998213 | | chr1 | 226997699 | 226998331 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I226810 | chr1 | 226997737 | 226998585 |
|
Enhancer Sequence | CCTCGTTCGA CCCCCTGGAT TCATTTAGGA GGGGTTCAGG GCAGATCTCC TTAGCAGGGC 60
AGTGGGCGTG GCAGCAGTGA TTGGCAGCTC TGAAGAGGTC TCTGCAGCCT GAGTATTTGA 120
GTGAGCTGGG AACTGAGGAA GGCAATACAC CAAGTATTCA GAATTTCCAC CGTGGACATT 180
GTTATGAGGC GACCTGAGAC TTCCCTTGTG CTTTAAGGCA GGTTCCCGGT GTTGGCATTA 240
TGCCTGGCAC GGGGTGCAGG TATATGGCCA CCAGGAGCAG TGGTGGTGTG TTAGAGTGCA 300
GAGGATGCTT GCACTCGCCC TGGAACATCT CCGCCAGCTC CTGCCGTGGC CTCCACTGGT 360
CCATCAGCAG CTCCATCTGC AGTCATTCAT GTTTGGCAAG TGGTGCTGCT GCCCCTGGGA 420
TGCAACCCAG GCCCAGCTCA GGGTGCAGGG AGGCTCCCAA GTGCTGTTTG ACTTGGACAC 480
AGTAGTCTCT GCAAGGGAGT CACGGGAAGG AGCGTGAAAT GATTCCAGAT TCCTGATTTT 540
CTATGGTATG ACAGGAGTGT TTCTCTGAGC CTCCTGATTC TCCTGGCCAC ATTCCCTGGT 600
TGGTTTTACT TCCTCGGGTC ATTTTTGAAG GGCCCTTGGC CAAAGCAGCT CAGAGGGGTC 660
ATGAGGCTGA ACAAAGGCTC TCCAGGAGGT GGGGGCTGAG TTTTCTCCTG CTTACACAAA 720
TGGAAAAATG GGGAGGTCAT TTGATTCCCA TAAAATACCC CTCCAAGCAG ACTGCTGATT 780
TCCAGCTAAC CACTAAAGAC TGGAGAATGC ATTCCAAGCC AGCTTTAGCA GTCACCACAG 840
AAATTGCCTG GTAACTGGTG GCAGCAGCTT GGCGGTGTGA TGTTGTGCTG AACAGCACAC 900
ATTTGAATAG CTTACTGAGT AGCTGAAAAG GGCAATGACC TTGACCCACT TTGTGATTTC 960
AGGTGCTTTT AAGAAGAACC CCATGCCAAG TGGAGGACGG TGTGAGAAAT GCAGAATGTG 1020
ATGGGGTAAC TTGGGTGGGT ATCAGCTTCC CATCAGCTGA CCAGTTCCCC ATCATCCCTC 1080
TCTGGGCAGC ACAGGGTCAC TGGGCTCCAT CTCCAGCTCA GGGAAAGTTC AGTGCAGCTG 1140
TGCCGGCTGT TGTTGGAAAT TTCATAATGT AAAGTGGAAA TTGGGCACAG GCCTCCAGGT 1200
GGTGGGTTCT TACCCCACTT GCCTTCTGGG CATCTGATGT GGTTTGGGTC 1250
|
