| Tag | Content |
|---|
EnhancerAtlas ID | HS118-10605 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr2:170617750-170619260 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr2:170618243-170618258 | AGTTAATTATTACCC | - | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 170618161 | 170618576 | | chr2 | 170618352 | 170618578 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I169761 | chr2 | 170617541 | 170619306 |
| Enhancer Sequence | ATTATAAAAA TTCAAGAAAA GAAGAAGTTG TGACACAAAT TTTATGGACT ATATAGCAAT 60
GAACATAAAA ATATGGCCAA CAGAACTGTC TTCTTAAAAT CCGGGGCATC GTCATACAGT 120
CTTTAACTCT GAATTGAATT TCGATGTTAT TTTGAAGTTG TGAGTCATAG ACTGTTAAAC 180
TCGTACTGGG GCCCTCTGAG TTAAAAGATA ATATTTTTGT GGGGGCCTCA CTGGACGGGT 240
GTTGAGCATC CTGCTCAAAC CTCCAGTGAA TATTGCAGAT CCCAACTGGC CGCCTCCTAA 300
GGGTGTTCTG AGCTGGTTTA GGAAGAGTCA CTGCAAATTG TGCCACGTTG GATACACAAG 360
ATTGCCAACA TTTCAACTTT TACCTTTGAA ATTCAAAACA GACCACAAGA TTGTATACCT 420
ACAAGTACCT ACAGAGGTTC TCGTTGGGAA ATCTGAAGTA CCAGCACTGT ATCCATCAGC 480
CTTAATAGAC TGTAGTTAAT TATTACCCAC TCCCCAACCT TTGTTCAGTG GCATTTAAAA 540
GTCAGGCTGA GCATGTATAA TCTGTGAACA CTTTCAGCAG AGACTTGTGA AATACATCTT 600
TCATTTGAAA GTTCACAGAC AAACTTTTGT TTCTAGTTCT TTCCTGGACA GATAAATACA 660
TAAAAGTGGT ACTTGTGGTT TCCCGAAGGT GTGTTTCTGC AGCCCTTCTC TAACCCTTTA 720
TAGCTTTTCC CTCCTCACAC CTTGACCATC AAGGAAATGA GTCGTACCTT CTTCCCTGTC 780
GAGAGAACAC AGGCCCTCCT TGTGCGCGGG CAGACATTTG AGATTAGAGC TTTACTAGTT 840
GTATGATTTT TTGAAAACTT TATTTACTGT TAAATATGAT ACGAATACAG AAATCCACAT 900
GAGACAAATG TACAGCTTGA GTTATTAAAG GGCAACTACC TTGCAACTGG CATCCATGTC 960
AGGAGAGAAT ACCTTGCCAA CTACCCCAGA CACCCTCCAC ATGTATCTCC TAAACCCTTA 1020
TCGATAACCT CTGTCTTCAC TATGGGGATT ATTTTCTTTC TCTTGGATAT TATCCACCTG 1080
TATTATGAGC ATCCTGTGGC TGCTGTAAAA AATTAAACTA GATGGCAACA GAAATGTGTT 1140
CTTTCAAAGT TCTGGAGCCC AGAGGTCTGA ATTTGAGGTG CCAGCAGGGC TGCACCCCTG 1200
GGGGACCTAG GGAAGAATCC ATTCTTTTCC AGCCTCCTGT GGTTGCTGGC ATTCCTTGAC 1260
TTGTGGCCAC ATCACTCCAA TCTCTGCTCC CTGGTCACAT TGTCTCCTCC TCTTCCATCT 1320
GTGTCAAATC TCCCTCTGCC TAACTCTTAT AAGGACACTT GTTGTTGGAT TTAGGGCCAC 1380
CAGGATAATC TAGGATGACT TTCTTTTCTT TTCTTTTCTT TTTTGAGGTG GAGTCTCGCT 1440
CTGTTGCCAG GCTGGAGTGC AGTGGCAAGA TCTCACCTCA ATGCAACTTC CGCCTCCTGG 1500
GTTCAAGTGA 1510
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