| Tag | Content |
|---|
EnhancerAtlas ID | HS053-00316 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:11443150-11444920 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LHX2 | MA0700.1 | chr1:11443674-11443684 | GTTAATTAGT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 11443709 | 11444800 | | chr1 | 11443705 | 11444695 |
| Enhancer Sequence | TGCTATTGGC ATCTAGTGGG TAGAGGTCAG AGATACTGCT AAACATCTTC CAATGCATGG 60
GACAGCCCCT ACAACAAAGA ATTATCTGGT CCAAAGTGTG AATAGTGCCA AGGTGGAGAA 120
ACTTTAGACT ACAGGGATCC AGAACATCCC ATCATTCCAC AGAACATCAC ACTGATCCAT 180
TATTATTATT ATTATTGAGA CAGGCTCTCT TTTTTACCCA GGCTGGAGTG CAGTGGTGTG 240
AACACAGCTC AGTGCAGCCT TGACCTTCTG GGCTCAAGCA ATCCTCCCAC CTCAGCCTCC 300
TGAGGGACTA TAGGCGTGTG CCATCATGCC GGGCTAATTT TTTATTTTTT GTAGAGACAG 360
GGTCTTGCTA TGTTGTCCAG GCTGGTCTCA AACTCCTGGG CTCAAGCAAT CCTTTCACTT 420
CGCCTCCCAA AGTGTTAGGA TTACAGGCAT GAGCCACTGC GCCCAGTCCA CACTGGTCCG 480
TGATATCAAT AAGACACATT GGCCCATTAT ATCAATGACA TCACGTTAAT TAGTCTGGAT 540
GGGCAAGAAG TGGCAAGTGA TTTGGAAGCC TTGATAGGAC AGACATGCTT CGGAAGGTGG 600
GGACTCCCTA TCAGTGAAAT TTTTAGTACA GTGGTTTGGT TTGGGGCACG CCAGGACATC 660
TCCTCCAAAG GAAACCACAA GTTGTTGCAT CTTGCACCTC CCACACATCA GAAGGAAACA 720
AAACATCTTA TAGGCCTTTT TTGGGTTCTT TAAGCAATAT ATTCCACACT TGACAAATAC 780
TGCTGCAACC CATTTTGCCA AGTGCCAAGG ATGGCTGCCA GCACTGAGAG GGGCCCAAGG 840
CAGGAGAGGG TTCTGCAGCA GCTCCAGGCT GTGGTACAAG CAAGTCCCAC GTCTGGAGTC 900
ATGTGACCCA GCAGACGTTG ATAACAGACA TATCTGTGGT GAGAAAAGAC GCTACGAGTT 960
TATGGCAAGT CCCAATAGGA GAATAACAAC ATAGATCCCT AGAGTTCTGG AACAAGGCCA 1020
TGCCATCTGT AGTGGAAAAT CATGCATTAT TCGAAAAATA GCTTTAGTGT GCTTCTGGGT 1080
CTTGATAGCG GTGGAGCGTC TGCTCAGCCT GGTACAGACA GCTTCGACAT GACACCCTGT 1140
GAGCATGGAG AGTCATCCCC CAGAACACAG AGCACACCCC AAATGAATGA CCATACTATT 1200
CTATGGTGTT GTGTCTGCAG TAGGTAAAAC ACGTGGTCTG GAAGCTAAGG GGTGAAAGTA 1260
ACAGAGCCAT CACTCACTGT CATCCTCAGT GACTCATTTA GGAAATTCAT TTCCTGTCCC 1320
TGAAACTTTA AGCTTTGTGC GTCTGAAGAT CTGCTCTGGT TTCCAGATGG GGAACGCTTC 1380
ACCAGGGTAT AGAGTAAGAG CTCCCCCAAA CTTTAACCCA CATCTGCCAC CTGGTCATTT 1440
CAGATTCCTT GGACCAAAAG GCCATGGGAC GAGGGAAGGA GTCACTGTAC TGGCAGGAAT 1500
TACTGTCCCT GAGCAACTGG CAGGAGAAGG TAGGATTGCT GTTACACAAT GAAGGCAGGG 1560
AAGATCAGTT TTGGTACCCA CGTGATCTGT TGGGCTGTCT TTTGTTATCC TCTTGCCCAT 1620
TTTTGACAGT AAATGGGTAA GTGTGGCAGC CATGAGCTGG GAAGGGCACA GTTACCAGGG 1680
AGGGGCCAGA CCTGTGAGGG ATGAGGGTCT GGGTCATCCC ACGAGGTGAA CTCTAGATCA 1740
GCAGAGATGC TCGCCGAGGC TGAGGGGAAT 1770
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