| Tag | Content |
|---|
EnhancerAtlas ID | HS147-03883 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:182972030-182973580 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA | MA0729.1 | chr1:182972140-182972158 | ATTGTCAAAAGGTCAAGT | + | 6.34 |
|
| | 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 |
| GH01I183002 | chr1 | 182972024 | 182972884 |
|
Enhancer Sequence | TTGCACCTAG GGGCACTATA GTATTTTAGA GCTTTTGATT GAGTAAGTCC CAAAACTACT 60
CTGGTAAGAG AGTTAAACAT TATTATCCAT GTTTCACAAT CAACGGCTTA ATTGTCAAAA 120
GGTCAAGTGG CTTACTACGA GTTAGTCAGT AGGGGAAAAA AGAGAATCTA GGAGTTTTTT 180
GTTTTTTTTT TTACAAAAAA AAAGAAAGGA AAAAGATTTC CTCAAAGTTA AATTAATGCA 240
CATAAGAATA TCAAAAAATA CAGCAAAGAT ACTTTGTCAA AACCAAGCAA CACTTAAACA 300
CAAAACATTA ATTTATGTTA ACTTTATGTA AGTAAGTTAT TTTGAAAGTC AACTCTAAAG 360
ATTATGTTCA GAAACTTCTA TTTATGCTAT TTTTGTTTTC TACACATTAT TTTAGTAATA 420
AGGGCTATAT CCTCCCATGA GATCTACAGG GCGGATATTA GATAAGCCAC AGATGAGTTA 480
ACTTGTTTTG GCTTGAATGA GGAAATGTGG CAGCTCCAGA TGCTTCCATG CTCCGAGCAC 540
ATCGGATCCA GTAGGCAAGA GAAACTGGGC TAAGACTCAA AGAAGGGAGG TGCTTTTAGC 600
TAATAACAAA GTCTACTCTT CCAGTGTTTC TGTAGGCAAG GATTTTTTTT TAAGAAAAAT 660
ATTATTACAA CATAGTTATA GATTCGTTCT TGGTAAACAA ACTTCAACAA AGGATGATCC 720
AAAAGGCTTG AATTTCTAGC TGCAGAAAGA GTTATTTTTA CTCTTCAGTC TGTTCCCGTG 780
ACTTTTTTCC CTACCTTTGT TAATGGCTTC ACCATCCATT GAACTGACCA AGCTAGAAAC 840
CTCAAATTTA TTCTCCACAG CTCCTTCTCC CTCACCCTCT TTTGCTACTG GTTTTAGTTT 900
TACTCATTCG CCCATTCTGT CATCTAAGTA GATATATTTA TTATATCTAC TTATATATCT 960
ACTATATCTA CATGTATAAC ACATCTGTTA TAACCTCCAT GGCCTCTTCT AAAGGTTGAG 1020
CCTCTCACCT CTCTGGACTA TATGACCATC TCCTAGATGG TTTTACTGCC CCTGATAAAG 1080
TTATTTATTT GCCTAAAAAC CACCAATGGC TCACCCTCAT CTACAGATCA GAATACAACC 1140
TCTTTAGCAT ATCTGCGCTC TCCCCAATCT GTATAATCAC CTATTTTCTT CTACTTCCCT 1200
GAAAACCTCT ACTCTGTCAG TTTCTTCTCA CCATTCCCCA GACATCTCCA GCATATCCAG 1260
CTCTTACATA TTTCAGTGTT TTTGTATGTG ATGTTCCTTT AACTTGCAGT CCTTCCTCTG 1320
CCTTCATTAC ATGACCAATC CTAAGGCTTC CTTTACTCCC AGCACAAATG TGGCCTCTCT 1380
CTCTGAAAGA TGTCTTGACT CCTCAAATAA TTAACTACTC CCATTTCATA TTTGTGGCAG 1440
AGATTCTTGC TCCTCATTGA ATAGAGTCTT TTGATGCTGC ACATTTGCCA GCTCCTTTCC 1500
AGTGCGGTAA GGCCATGTGA CTTCTTCTGG TCAAAGGGCT GTGAGTGGAA 1550
|
