| Tag | Content |
|---|
EnhancerAtlas ID | HS176-20935 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr2:73290550-73291970 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr2:73291502-73291513 | TGGGTGTGGCC | - | 6.62 |
| | | 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 |
| GH02I073062 | chr2 | 73289343 | 73292676 |
| Enhancer Sequence | AGAGTAAAAT GTAAATGAAG CAGTGCTTCA ATAGGCTCCA AGCAAAGCAA GACTGTGTGA 60
AAAGGAGTCA TCATAGGTCT GGACCAACCA CTCAGGGTCT TGTTTCCTTA AAAACTATAA 120
AGTTAAGATT AATGAGAAAC GTTGTGACCA GAAACCCCTT ATTTGCAGCT ATGGGTTGAT 180
TCTCCGAGGC AAAGTGACTT AGACCTGCCA ATCAAGAGGT AGATGGTTCA TTCCTAATGA 240
TATGACTTAA ACAGCAAAGT TCCTGGCAGT CTAGGACCTT ATAGAGTGAG ACATGAGTAT 300
GAAAGAGGTG GTTACTGGAA GAAGGTTGTT CGATACTTTA TAGATCCTGT GGGTCCTCGT 360
GAGAAACATT CTTTCTTTGC AGCTGGCTCT GTGTCTGTCC TCCCTGTCTG ATGAATGGCA 420
AGGAAGGTTA TACTTTCTCA GTCTCAGTTC ATTTTTATTT TCTCAATAGT TCAAAATGTA 480
TAGCCTCCCT CCCAAATTCA GCTCCCATCT TTACCCAATC GCACAATCGG TGGATGTTTT 540
TCCTCCCCTT TTTCTTTACT GGAAGAATGA GTCAGCCAAG TGATTCCTTC TCTTTCCCTT 600
CATAAGAAAG GTGAGTCAGC TAATTCTCAG CAGGAGCCAG GGCCTACAGC AGCAGCTGCC 660
TTCCCACCTC CACCAGCCAG CTCTCTCCCA TCTGCAAGCC CCCCAGGGAA GAGCAGGCCT 720
TGGGAGCAGC AGCAGAGGGC AAAGATCCCA GAAGAAGCTG ACACCGCCCC GCAACTACAC 780
ACACCAGACC TCCAAATTAC TGCTCTTCGA TTAGGAATAA TATACTCGCT GAACCTACAG 840
CCCAAAGCAG AAAGGCTGGG CCAGCCCAGT AGTCCTGAAT CAGCTGCACC CTGAACCACC 900
TGGGTACTTC AAAAACCAGG CCATACACCC AGGGATTCTG ATTCTATTGC TCTGGGTGTG 960
GCCTCCAGGC ATCAGTGTCT ATTTTAAAAC CTGCCCAGTG TGACTCTTGG AAATTATGAC 1020
CCCTCTCCAC TGCACAAACC AGCCCAGGAG CAGCACTAGA AAAAACTCAC TGTCTCGCCT 1080
ATAGGAAGTA AATGATTAAA ATATATAACC ACCTGCAAGG TACTGTGATT TTAGAACTTT 1140
ATTTCAAGCA AACTATGAGA CATATCCCCC CTGCCTCCCA ACTCTCAGCC CACACAAATC 1200
TCCCAACCTT GAAGTGAAGA AAGCATTTGT CTGCCCAGCA AGCTCTCCAT ACCCCAGAGG 1260
GAGCCCTGTG CAACCAGCCT GCTCTGCCCC ACTAGGCCTT GGTCCCCAGC ACACTCATAC 1320
CCCCAGTCAT CTCAGCAGAT AAGTGAGACT TCCAAAGGAG CAAGGAATTT TTGTTTTATT 1380
TTTGAGACAC AGTCTCACTT TGTCACCCAG GCTGGAGTGC 1420
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