| Tag | Content |
|---|
EnhancerAtlas ID | HS098-32002 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:166576480-166578080 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxq1 | MA0040.1 | chr2:166576720-166576731 | AATAAACAATA | - | 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 |
| GH02I165719 | chr2 | 166576484 | 166577983 |
|
Enhancer Sequence | TAAATTGACT CCATCATTAG AGCCAATTTA AACAATTCTT TAAATTTCCC CCTATAATTA 60
TATCCTTGAT CTTCTTGACA GTACAGGCAA AATTTTCCTG TAATTAACAA TGAGAGGGTC 120
AAGTCCCCTC TTGGAGGAAT TTATCAGAGT CTTTCCAAAC GTGGAACCTT TTGTTAGAGT 180
GAGTGTAAAA AAAAAGAACA AGAGGACCTC AGGACATGGG AGAGAAAGAA GGACAATGAA 240
AATAAACAAT AGCCTTAAAA ATAGAAGCGG AAAACAGAGC TAGGTGAGAA GATGCTGAAA 300
CTATCTTTAC TGAACACCGA CTCTTAAGGC TTTTGGTAAC TTTTTCTCTT CTCCCATCAC 360
AAAATAAATA TGAATGCCAA AGGGCAGGCA CACTTCCACT GTTGAGAGAA ACAGATCTAA 420
AAATAAGTAG GAAGCAGACA AGAACGAGCA ATGAACATGA TGAGAACCAT GGTGTCTACT 480
TTTAGGTTAA CTATGGAGGC ATGTAGGCAC AGATGGAGGA AGTTAGTTTA TCTTTGCTGC 540
TGCACTTAAA AAATAAAAAC CAAAAATATA AATGCCATCA AAACATTGAC TCTTCTCTAA 600
CCAAAATTTT TGGTTTTATA TTTAAGGCCA AGCCCATTTA GAAGAAAAGC ACATTCATTT 660
GGGTTTTGTG GTTTGGAGAA AGGACTGCCA GAGAGGAGGT GAAAGCCACA GTGGAGCATT 720
CCTGGACAAT CCATTGCAGG CTTGGGAGAT CACCATGCAG GCAGCTCCTG CTCCATAATA 780
GCCAAAATAG CAACATGACC ACAAATAATT CAAAGGCTGA AACATTTTGT TCCCACCAGT 840
TCAAACTCTC CTGCTTCTGT CAAATGGCTG GTAATCCTAT CTCCTCTACT AAGCCTTTCC 900
TAAATGAAAC AGTGGCAACT CCTTTTGAAT TCTACTATTT ATTACATAAA CACACAATTC 960
CCGTGGTTCC CTTATCACTC CATTAAATGC ACTTGCCCTC TGATTGAAAC ACAATGCAAA 1020
TCCTTTTATG CTACATTTGT TCAATGCTTG TTGCCTTGAC TGTATATAGC CTTAATATCC 1080
GGTAGGTGCT TCTAACTTAT TGTAAGTTCC ACATCTAATT CACAAAGTAT TTTGCTTAGC 1140
AATGCCTCTT ATGATGCAAA TAAACTAGTA TTTATCACGA GTGCTTTAGG ATACAGACAA 1200
GAAGACTATT TTAGAGAAAA TAAGAATTAA ATAATGGTAA GGAAAGCAAA CCACCCCTGC 1260
GATGTGCATG CTCTCCACCA CCACCCCTTT TCCCTCCCTG GATGGTGTCT CACTCTCCAC 1320
CTCCTTTTTG TCACTTGTCC TTGGTCACAC ATCAATCTGC CCTCAGCCCT CCAGAGAAGA 1380
CTTATTCTTC CTGCCTGAAA TGTTATTTCT CCCTTGTTCA TCTAACCTTG TTCCTTTTTA 1440
TTAAGTGCTT TATATATACG GAAGACTACA TAAATTATGT CTTCACGTTA AATAATAGTA 1500
ATACAATGAA CACCTGTGCA TCCACTTTAA GAAATAGAAT GTATCTTTGA AGTCTTTGTG 1560
TGTACTGTCA TGCTCGTGTC CTTCCACATT CCAAGGTAAC 1600
|
