| Tag | Content |
|---|
EnhancerAtlas ID | HS138-00551 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:28201100-28202230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr1:28202191-28202204 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr1:28202192-28202205 | AATTAATTAATTT | - | 6.92 | | POU6F1 | MA0628.1 | chr1:28202193-28202203 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr1:28202193-28202203 | ATTAATTAAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09233 | chr1:28198278-28207102 | CD14 | | SE_20343 | chr1:28199013-28203940 | CD56 | | SE_50884 | chr1:28199013-28201650 | Sigmoid_Colon | | SE_50884 | chr1:28201667-28202339 | Sigmoid_Colon | | SE_53500 | chr1:28198475-28202256 | Spleen | | SE_62491 | chr1:28184415-28220281 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 28201800 | 28202156 | | chr1 | 28201378 | 28202229 | | chr1 | 28201272 | 28202191 |
|
Enhancer Sequence | TGGGTAACAT ACTGAGACCG TGTCTCTACA CAAAATAAAA AAATTAGTCA GGTGTGATGG 60
TGCATGCCTG TAGTCTCAGC AACTCAGGAG GCTGAGGTGG GAGGATTGCT TGAGCCTGGG 120
AGGTTGAGGT TGCAGTGAGC TATGATTGCA CCACTGCACT CCAGTCTGGG CGACAGTGAG 180
ACTCTGTCTC GAAAAAAAGG ACGAGGTCTG TGTTGCCCAG GCTGGTCTTG AATTCCTGTC 240
CTCAAGCAGT CCTCCCACTT TAGCCTCCCA AAGTGTTGGG ATTACAAGCG TGAGCCACCG 300
CACCCAGCCA TAACTTCCAG TTCTGCCTCC TATTACCTGA TCATCATGTA CAACCTACTC 360
AGCCCCTGAG AGGCTGTTTC TTTTTCTTCT TCTTCTTTTT TTTTTTTGAG ATGGAGTCTC 420
CCTCTGTCAC CCAGGCTGGA GTGCAGTAGC CTGATTTCAG CTCACTGCAA CCTCCACCTC 480
CTGGGTTCAA GCAATTCTCC TGCCTCAGCC TCCTGAGTAG CTGGGATTAC AGGTGCCAAC 540
CTCCACACTG GGCTAATTTT TGTATTTTTA GTAGAGACGG GGTTTCACCA TGTTGGCCAG 600
GCTGATCTCG AACTCCTGAT CTCAGGTGAT CCCCCTGTCT TGGCCTCCCA AAGTGCTGGG 660
ATTACAGGCA TGAGCCACCA TTCCTGGCCA GCTGTTTCAT TATTTAGGAA ATTGAAACTG 720
CCTGTCTCCG CAAGAGCAGT CATGGGTCTT AAACACAATG ACGCATCAGT AGCCCTTGGC 780
ACAGTGCCGG GTATCTGTAG TACCACAGCT GCTGTTCTCA CCAGTCTGGA AGGCCCATGC 840
TCTGACATTG TAAACAGACT GTGGTTTATG ACTGGTGGGC ATTTTCCTGG CAGTACGTGG 900
GGAGGTTTTC ATCAGTTTCT CAGGGCTGAT GTTGGAGCTG CCCTGTGGGT GGGGCTGGGT 960
TCAGGTGGCC TCAAGGTCCT GCCACGTAGT CTGTTGTCCT CCATTAGCTG GATGGAGAGA 1020
CTGTGCACTC GTGTGTGCGT GAGAGATCTT TATTGAGCAA CTTCTGTGTT CTCGACACCA 1080
CTTACACACT TTAATTAATT AATTTATTTT TATTTATTAT TTTTTTTTTG 1130
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