| Tag | Content |
|---|
EnhancerAtlas ID | HS052-01211 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:45711550-45713060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx3-2 | MA0122.3 | chr1:45711854-45711867 | ATTAAGTGGTTTG | - | 6.1 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 45711683 | 45713049 | | chr1 | 45712438 | 45712809 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I045245 | chr1 | 45711581 | 45713411 |
| Enhancer Sequence | ATGGTAACCG AAATGATGAC AATGAATGAA ATCATCTAAG GAGAGAAGTT AGTGTGGCAA 60
GAAAAGAAAA GAGCTGAAGA AATAGCCCTA AAACACCCTA ACACTGGAGG ATGAATAGTG 120
GAGGAAGAGC CAGCCATTAG ATGAGGAAGA AGCAGAGATA TGTAATAAAC TCCAAAAGAG 180
AATGACAACA TGAAAGCCAA GAATAGAAAT TGTTAAATGC TGCTAAAGGC TGAAGCGTCC 240
CTTGGATTTA GTAACGAGAG GTTACTGATA ATAAGAGCAT TGGAATGATA GAAATGAAAG 300
ACAAATTAAG TGGTTTGAAA AGGGAAAGGC TTAGGACTTC TGATTTTAAG ATGGCAGAAT 360
GATTACTTAC AGTAGTCTCC AAAAAATATA AGAGACTCCT TTAACCCAAG CTTTGAGAAG 420
TGCATTGGTG AGAGGAGAAC TACCATCCTT GAAAGGCTCT GTATTGGCCA TTCTCTGCAA 480
GTCAGGAATG CCAGTGGGTG ATATTGTTTG GCTGTGTTCC ACTCAAATCT CATTTTGAAT 540
TGTAGCTCCC ATAATTCCCA CATGTTGTGG GAGGGAGCTG GTGGGAGATA ATTGAATCAT 600
GGAGGCAGTT TCCTCCATAC TGTTCTCGTG GTAGTGAATA AGTCTCACAA GATTGGATGA 660
TTTTATAAGG GGTTTCCCCC TTTCGTTTGG CTCTCATTCT CTCTTTGCCT GCTGCCATGT 720
AAGACATGCC TTTTGCCTTC TGCCTTCTGC CATGATTGTG AGGCCTCCCC AGCCATGTGG 780
CACTGTGAGT CCATTAAACC TATTTTTCTT TATAAATTAC CCAGTCTCAG GTATGTCTTT 840
ATCAGCAGTG TGAAAACGGA CTTCACTATC TTGCCTCAAG TCTGTGTTTA CTCTCCAACT 900
CTGTCATAAT CTAGATTGTA GAGACTTTGA TTGTATCACC TTTCCATAAC ACCTAACCAA 960
CTTCTGTAAG TAGTTGACAT TTTGCTGACT GTACAATGAA CAGGAAGTCA CATAACAAAT 1020
ACCCTGACTA GATGCTTTTG TAAGACACAT GCATAGCCTG GAGTGGAAAA TAAACATCAT 1080
AAAAGTTCAG GAAATTGCTA TGTTCTGAAT GTCTGTGTTC CCCCGCCAAA TTCTTATGTT 1140
GAAAATGAAT CACCAAGGTC ATGGTATTAG GAAGTGAGGC CTTTAAGAAG TGACTAGGAC 1200
ATGAGGGCTC TGCCCTCACG AATGGGATCA GTGCCTTTAT AAAAGAAGCC CCAGAGAGCT 1260
AGCTAGCTCT TTCCATCATA TGGGGATGGG GATACAGCTT AAAGATACCA TTTATGAACC 1320
AGGAACCAAG CCCCTACCAA ACACCAAATC TGCCAACGCC TTGATTTTGG ACTTCTCAGC 1380
CTCTAGAACT GTGAGAAGTA AATATCTATA TTTACTTCTT TATATAAGGA ATATCCAATA 1440
TCTTCATATA AGGTACCCAT TCTATGGTAT GATATTTTGT TACAGTAGCT AAACAGATTA 1500
AGACAAAGAC 1510
|
| |
|
|
|
