| Tag | Content |
|---|
EnhancerAtlas ID | HS095-16475 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr2:73290520-73292260 | 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 | AAAATATTTG GTATATAATT TAAGGAAGAT AGAGTAAAAT GTAAATGAAG CAGTGCTTCA 60
ATAGGCTCCA AGCAAAGCAA GACTGTGTGA AAAGGAGTCA TCATAGGTCT GGACCAACCA 120
CTCAGGGTCT TGTTTCCTTA AAAACTATAA AGTTAAGATT AATGAGAAAC GTTGTGACCA 180
GAAACCCCTT ATTTGCAGCT ATGGGTTGAT TCTCCGAGGC AAAGTGACTT AGACCTGCCA 240
ATCAAGAGGT AGATGGTTCA TTCCTAATGA TATGACTTAA ACAGCAAAGT TCCTGGCAGT 300
CTAGGACCTT ATAGAGTGAG ACATGAGTAT GAAAGAGGTG GTTACTGGAA GAAGGTTGTT 360
CGATACTTTA TAGATCCTGT GGGTCCTCGT GAGAAACATT CTTTCTTTGC AGCTGGCTCT 420
GTGTCTGTCC TCCCTGTCTG ATGAATGGCA AGGAAGGTTA TACTTTCTCA GTCTCAGTTC 480
ATTTTTATTT TCTCAATAGT TCAAAATGTA TAGCCTCCCT CCCAAATTCA GCTCCCATCT 540
TTACCCAATC GCACAATCGG TGGATGTTTT TCCTCCCCTT TTTCTTTACT GGAAGAATGA 600
GTCAGCCAAG TGATTCCTTC TCTTTCCCTT CATAAGAAAG GTGAGTCAGC TAATTCTCAG 660
CAGGAGCCAG GGCCTACAGC AGCAGCTGCC TTCCCACCTC CACCAGCCAG CTCTCTCCCA 720
TCTGCAAGCC CCCCAGGGAA GAGCAGGCCT TGGGAGCAGC AGCAGAGGGC AAAGATCCCA 780
GAAGAAGCTG ACACCGCCCC GCAACTACAC ACACCAGACC TCCAAATTAC TGCTCTTCGA 840
TTAGGAATAA TATACTCGCT GAACCTACAG CCCAAAGCAG AAAGGCTGGG CCAGCCCAGT 900
AGTCCTGAAT CAGCTGCACC CTGAACCACC TGGGTACTTC AAAAACCAGG CCATACACCC 960
AGGGATTCTG ATTCTATTGC TCTGGGTGTG GCCTCCAGGC ATCAGTGTCT ATTTTAAAAC 1020
CTGCCCAGTG TGACTCTTGG AAATTATGAC CCCTCTCCAC TGCACAAACC AGCCCAGGAG 1080
CAGCACTAGA AAAAACTCAC TGTCTCGCCT ATAGGAAGTA AATGATTAAA ATATATAACC 1140
ACCTGCAAGG TACTGTGATT TTAGAACTTT ATTTCAAGCA AACTATGAGA CATATCCCCC 1200
CTGCCTCCCA ACTCTCAGCC CACACAAATC TCCCAACCTT GAAGTGAAGA AAGCATTTGT 1260
CTGCCCAGCA AGCTCTCCAT ACCCCAGAGG GAGCCCTGTG CAACCAGCCT GCTCTGCCCC 1320
ACTAGGCCTT GGTCCCCAGC ACACTCATAC CCCCAGTCAT CTCAGCAGAT AAGTGAGACT 1380
TCCAAAGGAG CAAGGAATTT TTGTTTTATT TTTGAGACAC AGTCTCACTT TGTCACCCAG 1440
GCTGGAGTGC AGTGGCACGA TCATAGCTCA CTACAACCTC CACTTCCTGG ACTCGGGTGA 1500
TTCTCCCACC TCACCCTCTA GAGTGGCTGG GACTACAAGC ATGTGTCACC ACACCTGGAT 1560
AATTTTTATA TTTTTTGTAG AGACGGGGTT TCGCCATGTT GCCTGGACTG GTCTCAAACT 1620
TCTGGGATCA AGCAATCTGC CCACCTTGGC CTCTCAAAGT GCTGGCATTA CAAGCATGAG 1680
CCACCACACC TCGCCAGAAG TTGTTAAAAA ACTTCTTCCC TTCTTTCTGA GACAGGGTCT 1740
|
| |
|
|
|
