| Tag | Content |
|---|
EnhancerAtlas ID | HS095-02168 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:159566860-159569100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA | MA0071.1 | chr1:159567589-159567599 | TGACCTTGAT | - | 6.02 |
|
| | 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 |
| GH01I159596 | chr1 | 159566407 | 159569121 |
|
Enhancer Sequence | CATGATGGAC TATTTTCTAA AACACCCACA ATATTTCCTA GATTCCTAGT GGCAGTTCCC 60
TAAGTGTGCC AAAATCCCCC AGCCTGTTAG TGTTACTTGT TATTTAAGCA AAATGATTCA 120
AATCATCATT TGATACATGA TGGAAATCCC AGGCTCACTC ACCAAATTTC TAGCAAATAT 180
TGTGTGTGCT TGTAAGGGGG ATGGGAGGGC AGGAGAAGGC CTTGTATTTC TTCTAGTCAT 240
TACAAGCTAG TGGTTTTTCT TCCTCAGTCT GGAACTTACT CCTTGCACAT ACCTTTTTCT 300
GCACTGTGCC ATCATCCACT TCTCTTTACT TCCTAACTAC CACCAACTGA AAATTATACA 360
TATAAAAGCT TTAAACAAAG TCTCTTGAGG CTCTCAAGGG AGTTTACATT ACAGTATAGT 420
TCAGCAAACA ATTTTAAATC AAATAGTACA CCTCTTTATT CTTAGAATTC CCTCTGCCAA 480
AAAAGAAATC AGCTACTTTT TTTTAAATTC AAGGTCCAAC TTTCTGTTGT GTTGCTGATT 540
CTCTTCTCTC TTTTTCCAAC GACTTCCACT TCTCTCTCTA GTTTACATGT CTCCAAACCT 600
TAAGCCTCTG TTAATACTTT CACAATAAGT CAATTTTGCC AACGGTTTGC CTCCCCTAGA 660
CCATCTAGGC TGGGCCCAGA ACACCTCATC TTCACTCCCA CTGAAGTGTT CCTGAAGGTC 720
AGCTCTCACT GACCTTGATT CTGCTCCCCT ACACTGTCAC CAGAAGCTAT CCACCTATGG 780
TTCTAATTCA GTAAGTCCAA CTCTCTCACC CCCTTTTTTT GTCTCAGCTG TGTGGGCTTT 840
CCCAGGATGG CATGCAATGG GACCCCTGTG CCATGCATAT TGTAAAGGAA AATGCCTCCC 900
TCCATGCGCT ACAAAACAGC ACATTTATGA TGGCACTTTG AAAAGATATG GGTTGTGGTG 960
TCACATATTG ACAATTCCTT GGCCAGAGGC TTAACAGTGC CAGCAGTGCC AGAAGATTAA 1020
GAAGACAGCA AAAACAGAAA AGGGAGAAGA TGGTGAAGTA GTTATATAAC ATGAGCGAGA 1080
ATGCTCCTGA TTACAAAGCA GAGAAATTGA CTTTTTTTCT TAGTGTTTTC TATAGTCATT 1140
GCTCTATCCC TGTTCTAGAA TTCAAGTCAT GATAAGAATT TCTTCACGTT GACTTCCTGC 1200
ATTGCTTTCA GACATTGCAA TTAAAGAATG CGAAGAAAGA ACCTCACAGA GGTAACAGAG 1260
TTTGTTTTCC TGGGATTCTC CAGATTCCAC AAACATCACA TCACTCTCTT TGTGGTTTTT 1320
CTCATCCTGT ACACATTAAC TGTGGCTGGC AATGCCATCA TCATGACCAT CATCTGCATT 1380
GACCGTCACC TCCACACTCC CATGTACTTC TTCCTGAGCA TGCTGGCTAG CTCAAAGACA 1440
GTGTACACAC TGTTCATCAT TCCACAGATG CTCTCCAGCT TCGTAACCCA GACCCAGCCA 1500
ATCTCCCTAG CAGGTTGTAC CACCCAAACG TTCTTCTTTG TTACCTTGGC CATCAACAAT 1560
TGCTTCTTGC TCACAGTGAT GGGCTATGAC CACTATATGG CCATCTGCAA TCCCTTGAGA 1620
TACAGGGTCA TTACGAGCAA GAAGGTGTGT GTCCAGCTGG TGTGTGGAGC CTTTAGCATT 1680
GGCCTGGCCA TGGCAGCTGT CCAGGTAACA TCCATATTTA CCTTACCTTT TTGTCACACG 1740
GTGGTTGGTC ATTTCTTCTG TGACATCCTC CCTGTCATGA AACTCTCCTG TATTAATACC 1800
ACTATCAATG AGATAATCAA TTTTGTTGTC AGGTTATTTG TCATCCTGGT CCCCATGGGT 1860
CTGGTCTTCA TCTCCTATGT CCTCATCATC TCCACTGTCC TCAAGATTGC CTCAGCTGAG 1920
GGTTGGAAGA AGACCTTTGC CACCTGTGCC TTCCACCTCA CTGTGGTCAT TGTCCATTAT 1980
GGCTGTGCTT CCATTGCCTA CCTCATGCCC AAGTCAGAAA ACTCTATAGA ACAAGACCTC 2040
CTTCTCTCAG TGACCTAAAC CATCATCACT CCCCTGCTGA ACCCTGTTGT TTACAGCCTA 2100
AAGAACAAGG AGGTCAAGGA TGCCCTATGC AGGGCCATGG GCAGAAACAT TTCTTAATGC 2160
ATTATTCCTC TATATAAATA TACATTTAGT CATAGAAATG TGTGTCCTTA CTTACATTAA 2220
ACAACCTTAC GACTCTGTCC 2240
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