| Tag | Content |
|---|
EnhancerAtlas ID | HS064-00804 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr1:118196390-118198050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr1:118197806-118197819 | GAATTTTCTAGAA | - | 6.34 | | REST | MA0138.2 | chr1:118196490-118196511 | TCCAGCACCTGGCACAGTTCC | + | 6.39 | | STAT3 | MA0144.2 | chr1:118196408-118196419 | CTTCTGGGAAG | + | 6.14 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_10504 | chr1:118194357-118199851 | CD19_Primary | | SE_11059 | chr1:118192676-118211584 | CD20 | | SE_31627 | chr1:118197470-118198074 | Gastric | | SE_43509 | chr1:118193426-118209281 | MM1S | | SE_61007 | chr1:118138819-118218057 | HBL1 | | SE_62427 | chr1:118147317-118217904 | Tonsil | | SE_67143 | chr1:118193426-118209281 | MM1S |
|
| | 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 |
| GH01I117651 | chr1 | 118194205 | 118200237 |
|
Enhancer Sequence | TAGTTGTTGT CAGTCACCCT TCTGGGAAGT GATGGCTTAA ATGTCATTTC CTAAATAATT 60
CCTCTGGCTC CTGACCTGAG TTAGGCTTCC TGGCATCTTC TCCAGCACCT GGCACAGTTC 120
CAGATGCATA GCAGGAATGC AAACAAATGC TCGTCCATGA ATAAAGGAGA ATACCAGCAA 180
CTGGCTGTGT GACCTTGGGC AAGTCACTTC ACCTCTCTGT GCTTTAGAGT TTCCTCCTCT 240
GTAGTAGGAA GTAGGACTAT GTATCTCTAA GATCTCTTTC GGCTCTGGCA ATCTTTGGCT 300
CTTTAATGCT AGTGTCTGTA CAGGTTTCTC ATAAGGCTTC ACGGAATAAT GCAAGTGAGA 360
GCCTTGTTGA ATTGAAGGGG GAGGGGGAGG AGGCTAGGGA GCTTGGCAGA GGCAGCGGAG 420
TACCCACAAC GAGGCCCACT CACCCACTCA TTTCCTCAGC CACCCACGGG GCCTGCAGTC 480
CCCACGTGTA GCCTGATAGG CAGGGACTAG GGGACAGCCA GAATCAAAAC CACAGCCTCC 540
CGTTTTTAGT GTGTGGGCTT CAATTCGATG AGCTAGGGAG GAGACTTCTG GAGAAAAAAT 600
ACTCTGTAGG GTCACATACA CCCAGACAGT GTGGACACCT GCTACACACA CATACCAATA 660
TGTGCATTTA CAACTAATTA CATACAAAGG AAAGCACACA CACACCCAGA GGTGCACAAG 720
CACACGGTCA ATGCCCTGCA GAGCCCACCT GCAGCTCCCT GAGCCCAGGA CAGCTCTGTT 780
ACCCTCTGAG TCTCTGGGTC AATCTTTACC CTTGCCCTCT GGGTCTTCCC TCTCTCAACA 840
AACCCTGAGG CTGGGCACTG AGGCCTAGGG GATTCAGTGA TTTTACTGAT AAGGCTGAAA 900
ACAGGCAGGA AGGGAGGGTA ACTTACAGTG CTCTCCGGAT GTTACAGTAT TTGCATTTCC 960
ACAGTCTATG TGTCTGAAAA AAACTGGGTT TAGTCTAGAA ACTTGGTGGT ACGCAGGTGT 1020
AGCTTTCAAG AGAACTGGGA AACAATGCTG TATGGAGATG GTAACCACTT GTGAGCTGGG 1080
TCAGTTTCAC TATTTACTAT ACAGGCTGGC CATGATCTCA TTGAACTCTC AGAAGTGCCT 1140
TCTGCACAGA TAATTTATAG ATGATGAAAC TGAGACTTGG ACATGTAAAG TAATTTGCCC 1200
AAGGCATGCA ATTTGTAATT GGCAGATCTG GGACTCAGGG AGTAGGCTTC TGATTCCAAA 1260
GACAAGTGCT CTTACCACCC CTACCAGCTC AGCCTCTTGC CTCTGGTGTG TGCCCCTGCC 1320
CCCTCCCGCC TCTGGGCTCC ACATTCTGGC TGCTGACTCC CTCACACATG GCCTGGTGGA 1380
GCCCCTACCC ATGCTGAGTG GGGCTGGGAA AATGGTGAAT TTTCTAGAAA ATTGTGAAAG 1440
CGCTGCCTAC GAGAATGGCT GCCTGGGACA CTCCAGCTGC AGGCCCTGGG GCAGTGCCCG 1500
TTTGGAAGGT GCAGAGTTTT CTGGAGATAA GCAAACATGA GTCAGGAGAA AGCGACAAAC 1560
AGCTCACCCC TGCAGATTGG CTGCCAGGAC GTGAGATGAT CATGCAACGT CAAGCTAACA 1620
GCCTCAAATC TTTTTGAAAT CGAGTGCCCA GTTGACAGTT 1660
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