| Tag | Content |
|---|
EnhancerAtlas ID | HS141-01792 | Organism | Homo sapiens | Tissue/cell | NB4 | Coordinate | chr1:226661940-226663380 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx3-2 | MA0122.3 | chr1:226662835-226662848 | TTTAAGTGGATTT | - | 6.39 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CACCCACTCA CACGCCAGTC TCCTCTGGAA GCACCCTTGC AGATACACCC AGAAACAGTG 60
CTTCACCAGC CATCCAGGCA TCCCTCAATC CAGGCAAGTT AACACCTAAA ATTAACCATC 120
ACAGTTACTA ATATGGGAAA ATTGGAGGAC TACTAATAAA ACTCAGATTC TCAGCTTCTT 180
TTGATGATTG GAAGATCTGA CATCACTGTG CCCAGCTAGC TGAATGATAA TAGTTGTCTG 240
GGACAGAGTA ACAGCTGCCC TGCTAATAGT AAGAATAATA AGGATGACAA GAGCTAACAC 300
AGAGCTCAGA CAATGTGCCA GGCACGCTTC CCATGCAATT CACTTACCAT GGCCTCCTAG 360
GGCCCACTTC CCCTATTTAG GTCTCAGCCT GAGCCTGTAG GAGGCTCCAG GTGTTAACCC 420
TTGCTCCAGA GGAGGAGGGA AACCCTGGAA GGGGAAGCCC TGGGCCCCAG TCAGCCTCCA 480
GGCTGCTGCC CTGGGCTGAA AGAGCAGATC TTCTTAACGC TGTGCCAGCC ACTTTTCAGA 540
TTCATTTTAA TCTTCTCACT TCTGCCACTT GGCAGCTGCC ATCATACTTT ACTCCCTGCC 600
TGCTACCACT GCTTCTTGTC ACTTCCAAAC ACCATCAGCC TTTTGATCTG GCTTTCAGGA 660
GGGCAGAGGA GCTCCTTGAT TGGGGCCAGA CCCATTCACC ACATGTGACG GCTTAGGCAG 720
GACTTCGGGA GTGAGCTTGC TGGACTCATG TTGGTTTATT ACTTAGGGAC CTTGGGAGGC 780
AAATCCTTGA TGAAATCTCA TGCGGGGATG TAGCCTTGAT TTTAGCAAGG CATTTGATGA 840
AATGTCTCAA GTCCTACAGC CAAGCTGAAT AAATGTGAGC CAGCTGGTAG CAGGATTTAA 900
GTGGATTTTT AACTAGTAGA AAAACTGCAC CCAGACAGAT GAGATGATTG GATGCATGTC 960
AGTGTGGCTC ACTGGAAAGA AAACAGAAAA TATGTTTGCC ACGTGTTTAG AGGACAAGCC 1020
TTGAAACACC GAGGTGGAGA GTCTCCATCC AGAGACAGCA AAACCCCTTT GAAATACCAG 1080
CTCTGCCACA CACTGGCTGT GTGGTTGCGG GCAGACTTCC TCTGCCTCCC GGGGGTTGGT 1140
TTCCTCATCT ATTCAATAAG GATAATAGCA ATACGATCTC CAAGGGGTGC TGTGAGGATT 1200
AAATGGTTTA ATGCCCAGGG GACCTTCAGA AAGTGTCACT GTGGTAGTGA TCACGTTCAC 1260
AATGACAGGT TGCTATGGAG AAACTGAGAC AGAGAACTAG GCTCTGAGTC CTAATTTTTC 1320
CCCCAGTTAA GTTAGGTAGA TATGTGCCTA CCTCACTGTT GCAAACACTA AACTCTGTTG 1380
TCCACCTGGG ACAAAGGTAA ATGGGAAGGA TACTCACAGG TCTTAGCCCC TGTTGGGCAC 1440
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