| Tag | Content |
|---|
EnhancerAtlas ID | HS095-22854 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr4:104372160-104373200 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr4:104372775-104372786 | CCACACCCTCT | + | 6.02 | | NFAT5 | MA0606.1 | chr4:104372389-104372399 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr4:104372389-104372399 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr4:104372389-104372399 | ATTTTCCATT | + | 6.02 | | PAX6 | MA0069.1 | chr4:104372905-104372919 | TTCAAGCTTGAATT | + | 6.12 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTTTTCATCT TCTTACCTCC GTATTGTAAC CCTATTTCCA TAAAATAATA TGTATCATAT 60
TCTTTTTTCT TCCTTTGCAG CCTGTCGATG GCAAATATTT CCACTTGTGC TTCCCTTTAG 120
TTTCAAGACC TTTGCACTTG AAGTAATTGT ATCATAAGTT TCTTCTTTTC TAGCGTGTTA 180
TTCCCACCTG TATACAATAT GCTAATTCAT TTAAAACATC TATTCCTTGA TTTTCCATTT 240
CCCTAAAGAT ATTACTCCAT TTTTTGTAAT ATTGTTATCT TAACTTGCTC TCTCCATTCT 300
TCACCTACTG CTTACTAATC AACCTACTCC AATCTGGCTT CCATTTCTGC CATTCATGGA 360
AACCTCAGCC CATCTTCTCT CTTTTCTTTT CTTCTCTCCT GCCTCATTTC CTTTCTTTAT 420
TTTGCCAAGG ACATCAATAA TAACCACATT GCCAAATCTA ATAAACCTTT CTGTACTCAT 480
GTTACCCTGC TACTCAGGAG CATTCAATAT GAGTCAGCCT GCATTCCTTG AAAAACTTGA 540
CTGTCTAGAC TACTTCTTCC TTTCCAGTCT CCTTGTTCTG GATGATCCTT CCCCTTTACC 600
TGAAATCATA ATTATCCACA CCCTCTCCCT AGGTGATTGC ACTTAGTCAC TGTGATTTAA 660
ATGCTAACAA TTGAAAAACG AAAGAGCTCC AGACGTATAC ACCTACTGCT TATTGTACTT 720
GTCCAGTTGA ATGCCTACTA GGCATTTCAA GCTTGAATTT TACAAACCAG AACTTCTGTT 780
TTTTTTCCAC TCCCCACCTG TTCTTCGAAA AGTCTTCCCC ATCCCAATAA GTGGTACCAC 840
CAAACACCCA ATTATGCAAA CCCCAATACC TAGAAGTTAT CCATGATTTC TTTATTTTTT 900
CCTCATCCCC CCACAGCATC CATTAGCATG TTCAAAATAT ATTTTGAATC TCTCTGCTTC 960
TTTCCATTTA TACTGTTACT ACCTTGTTTT AAGTCACATT CATCTTTTCT GGACAATTGT 1020
GGCAGCTTCT TAACTGCTAT 1040
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