| Tag | Content |
|---|
EnhancerAtlas ID | HS118-10900 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:217604350-217606560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DMRT3 | MA0610.1 | chr2:217604667-217604678 | GTTGATACATT | - | 6.02 | | RUNX1 | MA0002.2 | chr2:217604988-217604999 | CTCTGTGGTTT | + | 6.14 |
|
| | 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 |
| GH02I216739 | chr2 | 217604439 | 217606418 |
|
Enhancer Sequence | TAATGCTTGA TGTGTGCCAG GCACTGTCCT AAGTGCTTCG CAAATATTAA CTCATTTAAT 60
TCTCATAGTT TGTCTATGAG ATATGTACTA TTGTTTATCC CATTTAAAAA CTGACATACA 120
GAGGAGTCAT GTTACTCGCC CAAAGTTACA CAGATACGTG GTAGAGTTAG GAGTCTACTG 180
GCCTGGGTTG CCTCCAATAT CTTCTGTTGT TACAGGACTT ACCTATTACT GGTTCGGCAC 240
ATGTGGAGGG GCCTGAGTGC CTGCGTGTGA TATTATGAAA GTAAATGGGT GCAACAATGT 300
AGGTACGGTT TGCTAGTGTT GATACATTGC AATCCACCCG TCCTTATTCC CCCTTTATAC 360
TGCCTCCCAG TTTCTTCCAG TCTCCCGCAG GCTATGCCTG CTCATGTGTC TTTCCCCTTG 420
TCCATTTCCC ATTCCTGTGC TGGACTGGGT TTCAGTGCTA TTTTTGCAGC CAAGCAGGTG 480
AGGTGGGCCT CTCTGGTGCC CTGCTGAGCC GCCAGGAGGC TGCGCCTGCA GAATGAATCC 540
CAATGCAGGG GTGGGGTTGC AAGCAGCATC CACAGTCCTC TTGTTTCAGT TCAGAATTGG 600
AGACGTCTGA CTGCCCTGGC TGCTGTGGCT TCTCAGAGCT CTGTGGTTTC TTCTGGAAAC 660
ACTGGGGAGA CCATAACAGC AGCACCGAGC ATCCCATCCC CACAGCCCAC CAGGTCCAGT 720
GGCTAACCTT CTTCTAGGCC ACTTTATTTT GGGTCATGGT GCTGTCAAGG CTCTTCCGGT 780
CCAGGAGAGC ATGGTCTTTG CAAATGCTCT GCAGAGCTGG CCCTTCTCGC AGGAGTGGTG 840
TGGATTATTT GCAAAAACAA CAGAGACTCT GCTAGCATTC CCACAGATAA CACAGGGCTG 900
CAGAGGAAAA CGTCCTCTTT GCCAGCACAG GCAACAGGGT GGGGGACGTA GGGGCAGAGA 960
GGAAGGGTGT GCTGTTTCTT CAGAGTTCAC CCCATCCATT CCCCACATCC AAATAGTTCA 1020
GCTTAAATAG TTCCCAAGCT TAAATGAACC TCTTGCGGTA CCCTTCCTTT GCGAAAGCAC 1080
CTGGCAGTGG GGCAGTCCTT CTGATATTTA ACAGCTGGCC CTCCTGCTTC AGGACTACCC 1140
TTTGTGTTTT TCATGGATGT TCAGCACAAT GTGCTTCAGA TACAGAGGAA AAGCCAACCA 1200
TACATGGATC TGCTGCCCCT GACAAAGGAT TCCCACACTG GGAAGGGGTG CAGGCTTCCT 1260
GTGTACAGGT TTGGAAGAGC CCCTGTGACT TGATATCAGG CCCACTAGAC TCAGGGCCCT 1320
TTGGCTCCTG ATCTTCCCCT CTTTGAGTCA CAAAACTACA TACCCTGCTC AGTCCCTTTA 1380
AAGCGTACTT TTTCCCTTGG ATTTTTTTTT TTTCTCTCTT TGGTGTTTAT GTGAACTGGT 1440
TGAACCCATC ACGTGGTGAG TCCATGTTTA TAATTGCAGA AGCACTGCCT GGGGAAGTTT 1500
TGTTTGTATA GAGGTCATCT CATCTCTTGG GCTTGGCTGC AGCCCCAGCT GGGGTTTCGG 1560
CAGCAGTAGC TGAAAACACA CCAGGGACTT CTTATTTCTC TCTCTGCCCT GGGTTCCAGG 1620
CTCCTGGTCC CAAAGGCTGG TGCTTCCTAG GGCAGGAAGA AGGGGCACAC TCAGGAAAGA 1680
GCAGGATCAT CTTCCTTCCA CCCCATGCTC AACCCAACCT AGAGTTTTTC CAGGATATGA 1740
CTGTCTCCTT TCTTACAACC CGACTGCTTT CCATGGTCTG AAAGCTAGAC TTAGATTGGT 1800
AGAGTAGATG GTAGGATTTA GGGATGTGCT GTTCTGTTGC TACTCTCCCT TTTACAGTCA 1860
ATATTCTAGG ATGGCTGAGA CCATGAGCTT TGGAGTCGGA CAGAATTGGG TTGAAATCAT 1920
GTCTTTGCCA ACTACTAGCT GTGTGACCTT GGACAATACC TCTAAAACTC AGTTTCAACA 1980
TCTTAAATGA GAATAATAGT ATCTACACCT TCAGATGGTC AGCAGGATTA ACTTAGGGCA 2040
TGGGTATGAA ATGTTTCTAA TTATGATAAT AACGATGGTG GTAATCAATA ATAACACTAA 2100
CTATGATAGC ACTAAAAATG ACAACTTCCC TCTATCCCTG TTTCCCTCCT CTATTAGAGC 2160
AGTGTTTCTC AACTTTTTAA AATTATCACT CCCCTAAGGA GTCTTTTAAG 2210
|
