| Tag | Content |
|---|
EnhancerAtlas ID | HS147-36700 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr6:119467860-119469350 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr6:119468653-119468664 | GGATGACTCAG | + | 6.32 | | JUNB | MA0490.1 | chr6:119468653-119468664 | GGATGACTCAG | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACAAATAAGG AATAATGTCA GCATAGTATG GGGGTTGTTG GTCGACATGT ATCTTTTCCC 60
AGATGAGAGA TGCTGTAAAA ATGGGAGTAG AGTTAAAATC ACTAGCAGGA AAGGAATAGT 120
CACCCTCTCC CCTGGTGCAC AGATTGGAGC TCTTCCAACT CTCCTTGAAT TAAAAAGGAG 180
TGCCTGTACC CAGGGTTTCC TCCCAGAGAT GTGCACCCCC AGGCTTGCAT TTATAGCTCT 240
TGCCCTTTCC ACATGATAGT CACTACATTC CAGAAAAAAA CAAATGTAGT TTATTATCAG 300
GATAGAGCCA GGGCCCCAAA CCCTAGTTAG AGGCACTAAG ACATCCAGCG GGGGCAGTGG 360
CAGGCTCTGT TTTTTTTTTT TTTGTTTTTT TGTCTCCCAG ATGCCTACAA AATGTGCCAC 420
CCTAACATCA ATACCACGAA CACAAGCACC ACTTCCTCCT CTTTCTCCTG AATCTGAAGT 480
CTCTTCCAAG TTCCTCATCC AGTCATGACT AAGGCAGCAA ATAATCAAGT TGCTTCAGCT 540
ACATAGTAGT GGCTGGAAGA GGGTTTAGCG TGGGTGCATC CTAGCTGTGG GTCTGATCGA 600
TGATACAACC TGGTATTAAC CGCTGGGCTT CCAACTGGTC CTGTCCCCTT GAAGACTTGA 660
TTCTGACTGG GGATAGGGTG GGGTGGGTGG GGCCTTTTGC CAATTCCAAC TCCTCATTGT 720
TTGCTGACAT AAGATGAGGG CTCCCAACCC CCACCACCTC TTGCCAGGCT GATCCTTGCT 780
TGAGTCATAG CAGGGATGAC TCAGAGATGA TAGACTGAAT CTAGAAACAG ACCAGACCAC 840
ATGTAAAAAT AGATCTTTGA CCCACTCTCT GTACCAGAGA AGGAAACCAA CCCCCTTATG 900
TACAATAAAT AACCCAGGAA GTCAGCCTGC TCGAACTCAG ACTTGTAGGA AGCCAGGCTG 960
CTGTCTCTGG TGACAATCCA GGAAGCTGAA CAATAACTTC TGTAACAATC AGCCAGAAAT 1020
GGCCAGGACC TGATTAATAA CGGACAGCTT CCCTAACTTT TGTCACCATT TTAAATTTAG 1080
GAACAACCAG AGAAAGCCAA ATCTGTACCT ACCCCTAACC AATCACACAG TGTGCCCTGC 1140
TTCCAGTTAG CCCACCTGCA GCTTCCCCAG GCCAACAGCC TCCCATCAGG GCACACCTCA 1200
AGACTTCCCT TTTTTTCCAC TCTAAAGCTT TCCCAGTGCT TTGCCTGTGA TGGGGTCTCT 1260
GACAAAATGC AAGTGATGGT GGCCAACTTC ATTGCTATAG CAAGCTCAGA ATAAATAGCC 1320
TTTGCTTTTT CTCATTTGGT TGGTCTTTGT CTATTTCCAT GGAACCTATA ACCTGCTTAC 1380
TGTCAACCCA CCCACCCTAG TTCCCTGCCT AGCAATGAAA CTCCATACCT CAACTTCTCC 1440
TATATGGACA AGATTTCTTC CTCTGCTGGG AAGAAGATCG TGGCCAGGAG 1490
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