| Tag | Content |
|---|
EnhancerAtlas ID | HS037-34709 | Organism | Homo sapiens | Tissue/cell | ESC | Coordinate | chr6:154300100-154301450 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr6:154300517-154300533 | GCTTAGGTAAACAAAG | + | 6.31 | | NFE2L1 | MA0089.2 | chr6:154301332-154301347 | ATTGCTGAGTCACAT | - | 6.79 | | NR2C2 | MA0504.1 | chr6:154300756-154300771 | TGACCCCTGACCCCC | - | 7.06 | | ZNF263 | MA0528.1 | chr6:154300951-154300972 | CCCCCTCCCTCCTCTTCCCTC | - | 6.93 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTTATTTTC TCTTTTTCCT TCTTTTATAC TTTCAACTTT TATTTTAGGA GGTACCGGGT 60
TCATCTCACT AGGGAGTGCC AGACAGCAGG TGCAGGACAG TGGGTGCAGC GCATCATGCG 120
CGAGCCGAAG CAGGGCGAGG CATTGCCTCA CTCGGGAAGC GCAAGGGGTC AGAGAGTTCC 180
CTTTCCTAGT CAAAGAAAGG GGTGACAGAC GGCACCTGGA AAGTCTGATT ACTCCCACCC 240
TAATACTGCG CTTTTCCGAC GGGCTTAAAA AACGGGGCAC CAGGAGATTA TATCTCGCAC 300
CTGGCTCCAA GGGTCCTACG CCCACGGAGT CTCGCTGATT GCTAGCACAG CGGTCTGAGA 360
TCAAACTGCA AGGCGGCAGC CAGGCTGGGG GAGGGGCGCC CGCCATTGCC CAGGCTTGCT 420
TAGGTAAACA AAGCAGCCGG GGAAGCTCGA ACTGGGTGGA GCCCACCACA GCTCAAGGAG 480
GCCTGCCTGC CTCCGTAGGC TCCACCTCTG GCGGCAGGGC ACAGACAAAC AAAAAGACAG 540
CAGTAACTTC GGCAGACTTA AATGTTCCTG TCTGACAGCT TTGAAGAGAG CAGTGGTTCT 600
CCCAGCACGC AGCTGGAGAT CTGAGAACGG GCAGACTGCC TCCTCAAGTG GGTCCCTGAC 660
CCCTGACCCC CGAGCAGCCT AACTGGGAGG CACTGCCCAG TAGGGGCAGA CTGACACCTC 720
ACACGGCCAG ATTAAGCGGT ACGTGTACAG GTTTCTTACA CAGGTATATT GTTCGATGCT 780
GATTTGGGAA TGAATGATCC CATCACGCAG GTGGGGAGCA TGGTACCCAA CAGTTAGTTT 840
TTCAGCCCTT GCCCCCTCCC TCCTCTTCCC TCTAATAGCC CCCCGTGTCT ATTGTTGCCA 900
TCTTTATGTT TACGAGTATC TGACGTTTAG CTCCCACTTA CACATGAGAT CATGTGGTAT 960
TTGGTTTTCT GTTCCTGCAT TAATTTGCTT AGGACAATGG CCTCCAGCTC TATCCATGAT 1020
GCTGCAGAGG ATATAATTTC ATTCATTTTC ATGGTTGTGT AGTATTCCAA GGTGTATATT 1080
ACCACATTTC CTTTATTCAG CCCACCATTG ATGGGCACCC AGGTTGATTC CATGTCTTTG 1140
CTGTTGTGAA CAGTGCTGCA ATGAACATAT GAGTGCATGT GTGTTTTTGG TGGAATGATT 1200
TATTTTCTTT TGGATATATA TCCAGTAATG GGATTGCTGA GTCACATAGT AATTGTTTTT 1260
TCTTTGAAAG ATCTCCAAAC TCTTTTCCAC AGTGGCTTAA CTAATTTACA TTCCCACCGA 1320
CAATATATGT GTTACCCTTT TTCTGTAGCC 1350
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