| Tag | Content |
|---|
EnhancerAtlas ID | HS148-14064 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr5:34761890-34763260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr5:34762639-34762660 | AAAAAAAAAGTAAAAGCAATT | - | 6.67 | | Nr5a2 | MA0505.1 | chr5:34763203-34763218 | GCAGGCCTTGAACTT | - | 6.34 | | Sox3 | MA0514.1 | chr5:34762092-34762102 | CCTTTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_45592 | chr5:34761818-34764052 | Osteoblasts |
|
| | 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 |
| GH05I034761 | chr5 | 34761335 | 34764413 |
|
Enhancer Sequence | ATTCGATTAT TTTATTCTAT TTATTTAGAG ATGGGTCTTG CCATATTGCC CAGACTTGAT 60
TTGAACGCTT GGCCTCAAGT GATCCTCCTG CCTCAGCCTC CTGAGTAGCT GGGACTATAA 120
GGCATGCACT ACCACACCCA CCTTTATTCT ATTATATCAA ATGAACAGGA ACGACAACAG 180
AAATGTCTCC ATTCTAAGAA AACCTTTGTT TTCTGAAAGA CTTGAATCCC GTAGAGTACA 240
GTAAAGCTCC CTAAGGACAG GGATGGTACA ATCTTATTGT GTTGGTCTTT CCCATTGTTC 300
TAGGCCCAAA GGAGGCCTTC ATTTGGGATT TGTGTAAATA ACTTTTCAGT GTGTTCTTGT 360
GGAGAAAACA TTCTTTTTTT GCTGATAATA TCTTATGGGT AAATTGCTTA GGGGTGAATT 420
AACTTGGATT CAGAGGGGAA AGAATTCTTC TGGTGAACAT CACAACCTGA CTTGGCCCCC 480
AAGCTTCCAC GGCAATTTAA ATAGAGAAGT ACTCAACCTT TACCACCTAG AGAGCCAGGC 540
AGTCTAGAAA GTCCCAACAA TGTGGCAACA AAGGCAGCCA TCTCCACAGA CGTTCTCCAG 600
AAGCCTCCAT AACCCAAGGT CAATAACCAG ATGGGTGGTT GGGTAATGCC TTAGACTTTT 660
GAGTTTCTTT CTGGAGTATT TTCTTTCAGG GAAAGATGAG AATGCATGCC AGGAAATTTT 720
CTTCCTCTAA GACTGATCAA AGAGGGGTTA AAAAAAAAGT AAAAGCAATT GAATGACTGG 780
AATTCATTTA GGAAAAGAAT AAAGGAAGGG TGGTGTCTTG GGTAGGAAGG GAACAAAATA 840
GAGCAGAGCC AAGAGTTATA GCTGCAGCCT GTGTTTATGG AGTCAGGCCT GGCGTGCCTC 900
TGCCCAGCTG TTCTCTTTCC ATGGTGGATG TGAGGAAGTG GGAGGAGGTC AATGTCCTCA 960
AACCTCTTAC CGTAGAAGAG TCTAATTGTT TCAAGATGGG TTCCCTACAT TTGGATGTGC 1020
ATTTAATTAA AGTTATGTGT GTTTGTCTTA CGAACAACCA GACTAAATAA AATCACTGCC 1080
GGCACTGTAG TATTTGAACA AATACCACCT GGGCATGTGT GTGTAGATAT AAGGAGTGTG 1140
TGCATGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TATGTGTCTG 1200
TATCATTTTA TGTTGCCCAC TTTTCAGAAA CCTGATCTTT TTGGCTATGA AAGCAAGAAT 1260
TTGTGAGAGT ATTTTTAGAT GACTCTGTGG AGCTTGACTA TAAAGTGGGA GAGGCAGGCC 1320
TTGAACTTTA GAAATCACTA TAATAAGGGC TTCTCTGGCT GGTGGTTTGT 1370
|
