| Tag | Content |
|---|
EnhancerAtlas ID | HS113-14727 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr16:89698700-89700350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr16:89699049-89699060 | ACAGATAAGGA | - | 6.14 | | ZNF263 | MA0528.1 | chr16:89699356-89699377 | GCAGGAGGAGGAGGGAGGGGA | + | 6.15 | | ZNF263 | MA0528.1 | chr16:89699362-89699383 | GGAGGAGGGAGGGGAGAGCAG | + | 6.49 | | ZNF263 | MA0528.1 | chr16:89699359-89699380 | GGAGGAGGAGGGAGGGGAGAG | + | 9.53 | | Zfx | MA0146.2 | chr16:89698704-89698718 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 89699468 | 89700263 | | chr16 | 89698855 | 89699182 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I089631 | chr16 | 89697242 | 89700208 |
|
Enhancer Sequence | TCCGCCCGCC TCGGCCTCCC ACAGTGCTGG GATTCCAGGC GTGAGCCACC GCGCCCGGCC 60
GGGGGTCACA GTTGTTAGAA GCTGTTACGG GACCCACCTT CATCCCTTGG CCACCGCCAG 120
CGACACAGGG GCAGGAAGTA TCTTCAACCC AAATGGCTGT GTGCCCGCTA AAAACGGGGG 180
GTTTTAAAGT CACAAAGGAA AAGGAGGAGA ATGGATCCCG GGGGCAGCCA GCAGTCTCCC 240
CACGAACAGC TGCCTGAGTG TGTGCTTGCC GCTTTTCCAG CACTTTCCAG CACTCCTTGG 300
AGCAGGACGC CGGCTTCCAT ATCCCAGCTA AGGGCATTGC CCCAGCTGCA CAGATAAGGA 360
GGGTGGGTCT GATTAGCAGA ACTGCCATTT GCCCTGGCCA TGAGGCAGGC AGGGCCTCCC 420
TCCCACTGAG AAACCAGAGG CCCCACCTTC CCATCGTTTT CTCCAGCAAG AGTGGAGAGG 480
GCTGGCGGGG CACAGTGGCT CACAGGTGTG GTCCCAGCAC TTTGGGAGAC CGAGGTGGGA 540
GGACTGCTTG AACCCAGAAG GTTGGGGGCT GCAGTGAGCT GTGATTGCAC CCCTGCCCTC 600
CAGCCTGGGC AACAGAGTGA GACCCTGTCT CAAAAAGAAA AAAGAAAGGA GGGGCTGCAG 660
GAGGAGGAGG GAGGGGAGAG CAGAGAGCTG CCCCATTGCA GCCTGTCCCT CCAAGGGCGG 720
CTCCTGGGGT CCTAGGAATC CCTACCCATC CCAGGCTAAT GTCTGAGATG GGCCGCCTGC 780
GTCCTCAGGC CAAGGAGTAA AGTCTCCTGG GAGCCCTGCC CAGCCCCACC CAGGACAGTG 840
CCCAGTGTAG GGTTGCACCT AGCGATGAGG CTGCTGCCCG GGCAGGGTCC CTGGCTGGAG 900
CTCATGGTTC CCTCAGCAAG TGCGTCCTGA CCACCCACTC TGCTCCGAGG GCTGGGGAGA 960
GGCCCGTGCC AGCCCAGGCT GTCATGTGGA CTCGCTGTGG CCAGGGACAA CCTCGCTGAC 1020
GCAGGAGCTT TGGGAGAGAC TCACACCAGC ATCAGGCGTG CGCCCGCCCA TCTGCCCAGG 1080
GGTGGGGCCG GAAAGCGTGC CAGGCTGGGC TTGGGGGCAC TAGCCCAGGG GAGGTCAGGA 1140
ACGACTGGGA CCCAGGAAGG GCAGAGCCCT CCCCTTCTTT CCCCTGAGGA GCTCCATGGG 1200
TGCATTCGCC TTGGAAAAGC TCATTGCGGG CACATAGATT TGAGCTGGGT CACAGAAAGC 1260
AGAGCCCGCA GCTGGAAATG ATTAACAGTT ACTCATCTGC CTCTCCCAGC TGCCCTCCAA 1320
GGAAAGCACC AAGACACCCT CATGTTACAG ATGGGGAAAC TGAGACACAG AGGGAGCTGT 1380
CCTCAAGGAG AGCACCAAAA CACCCTCATG TTACAGATGG GGAAACTGAG ACACAGAGGG 1440
AGCTGTCCTC CAAGGAAGGC ACCAAGACAC CCTCATGTTA CAGATGGGGA AACTGAGGCA 1500
CAGGGATGGG TCTGGAAACT GCAAGTGGAG GGGCCCCTGT GGCCTCATCC CAGCGCACAC 1560
CCTCACAAGG CAGTCCCCCC GAGACAGGGG CACAGCCCAC ATTACAGGAA GGAGACTGAG 1620
GCCCCAGACC CAGTGACGGG GAAGGGGAAC 1650
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