| Tag | Content |
|---|
EnhancerAtlas ID | HS076-01832 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:37311180-37313920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr1:37312922-37312938 | CCCAGTGTAAACAAAT | + | 6.04 | | Myod1 | MA0499.1 | chr1:37313206-37313219 | AGCAGCTGTCACT | + | 6.64 | | POU2F2 | MA0507.1 | chr1:37313008-37313021 | AAATGCAAATTAA | - | 6.25 |
|
| | 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 |
| GH01I036847 | chr1 | 37313501 | 37313670 |
|
Enhancer Sequence | CTGAAGCTCC TTTCTGACAG GTAACGTCAG CCCATAGCCA CACATGCACG CACAAGTATA 60
TACAATGTCC TTGGCACAAA TGCACCACAT TTTCAGATGT CCTGTCTGCC TAGCCCTTCT 120
CAGACACAGA GGCCAAGGAC CTTGGACCTG AGGCCTTGGC TTCAACCAGT TAGAACCAGC 180
ACACAGTATC AGGAGTCCTA TTCTCCCAGC AGGAGGGGCC TAGAATCGTT CCCAGCCTGG 240
GATAGTTCTC CCAGCCAACA CTCTAGCCCC AGGTTTTTCC CCTCTCCTGC TGCTGGGTGC 300
TGAGTGTTGG GCTTGCCTGG CAGGCAATTG AGCCTATGTG GGTCACGATG TGCACACGGC 360
ACAAATGCAC CCATCACTGA GTATCCAGAT ACCCGTGTGT AGCTGGTCCT ACACCCACCC 420
ACACACCCGC ACGCATGCCC ACACCGTGAC ACCATGGCTC ACATCGGCAG CCAAACGAGT 480
CTTGAACCTT CAAAAGCTGG GCCCCCAAGA GTGGGCCGGG TGTGTTTTCT CAGTGTGTGA 540
GCTGAGGTTT GGGCAGATGA ATTTTTCATG AGCTCGTGGA AGAGCGGAAC CAGAACAGAG 600
GCTGGGGCCG GGCGGTGAGA GGGCGGGGGA GGGCAGGCGT CCAGTCTCCT GCTGCTGCTG 660
TTTCCATCTC AGGAATGGGG AAGGCTGCCA GTGGCTCTGA GGGGCCAGAA AGGGCAGTGC 720
CAGGGCTCTG TCCATCTGTC TGTCCAGGGT AAGGCATCTT TAGCACCTAA CGCTGGGGGT 780
TTAGGAGAGG GGAGAATAGC AGGTAGGTTT GGTGGCAGCT CACACAGAGC TGCTGCTTTC 840
TGCCACACCA GATTCCTGGG AAAGAAAGGG GAGGAGAAAC TCCCCCTTAT CAGGGGTCTT 900
GGATCCAGGC CCTGTTCCCT AGAGGCAGAG CAGTTTGATG TTGTGTACTG GTACCTTGGG 960
ACCTGCCTGT CACTCAAAGC ACTGTTGCCC TGACAACATC CTCCCAGACA GGCTGGGGCT 1020
GTGCTCTCAG CAGGAGGTGC TGGCCCTACA TTCAGGCTGC GAAGCATGGG GTTGGATTTT 1080
CAGCCACAGT GGCTGGGGCT GGGCCACTCC CTGTCACCTT TTAGCTGTCC CAAAGAGCCC 1140
AAGCCTGAGA GCATCCCCTA GGGCTCCAAG ACATGCAGAC CATGCAGAGC CTTTTGGGAA 1200
CATTCTCTGG AGCATCTGGA GCAGCTCTAG TTTCAGGGGG CCCTAGGCCA GTCCTTGCAT 1260
GGGAGCGAGC ATCTCTCCTC AGGAGACTCC AAGGACACTT CTGGCTAGAC AGACTTTCTT 1320
GGAAGCCCAT GTAAAGACTG TGTCACATCC TCTATCCCCA TCAGGGATAC TCCAGAGGTC 1380
ATTCCCTCCA TTCCCCTGCC TCCAGGAAAC AGTAGGCTTC TCTCACTGCC CCATAGGGGG 1440
AAGCACACCT CACCCTCCGG TGATCTCTGG GCAGTGGGGA TGGAGACAGC TGAATCATCA 1500
GTCACCCCCA GGCCATGTGA GTATTTGATA CTACATGATG GGGTTAAGAT GGTCAGTGGC 1560
CCCATCCATA GGCGGTGGGA TATCTGCTTC AGGAGCTGAG ACCGTGGCCA AGGTAGAAGG 1620
TGAGGTGGTG GTTGATCTGG AGTTCTATAT CTCAGTAGGA GACTAGGACT ATGAGGGACC 1680
CATGAGGCTG CAAACCCTAA TGCCTCCAAT GGCCAGCTGA GAAACACAAC TATAAGAAGC 1740
AGCCCAGTGT AAACAAATAG GGAGGGCTCG GGGGCAGAGT GGGGGACTAT GGTGAGCCAG 1800
GGAATGGCCA TGAAACTGGA AGGCACTCAA ATGCAAATTA AGTTTGTAAC AGAACAGCCT 1860
GTGCTAGAGA TCACCTCTGT GGCCATGGGC AGGGGTCTTT GGTGAAGTTC AGGGCTCTGC 1920
CTGTGGACAG AAGTGGAGAT TTTCTCAAGA TCTCTCACTC AGCATGCTGT ATTCAAGCTG 1980
AGCTCACTGG GGACTGGATT TGTAATCAAT AATAATGAAT AACAATAGCA GCTGTCACTT 2040
AGACCGCACT CTGTGCCACT TAATTAATCA TTCATGCTCT GAACTCTATG AAGTAGGTGC 2100
AGTTATTAAC ACCTCCCTTT TTCAGGTGGA GAAACTGAGG CACAGGGCGG ATAAGCAATT 2160
TCTTAGGGTC ATATGGCAAA TCAACATCAA AGCCAGGACT CCACCCCAAA GGTCTGTGCT 2220
TTTGATCATC AAACTGTTCT TTCCTCATGT CCTGGTGGCA CTGCATGTCC CAAAGAGCTC 2280
TGGGGTTGTA TCTGCCCAGA TGCCTTGCAG CTGAGAGGCT GTGGGACAGA TGGAGCTGTG 2340
ACCAGGCTAT GAGCCAAGAG GGGTTCTCTG CTTTCCTAGC CCTGGGCTAC CTAGGAACCA 2400
GCAGGATACT GGGAATGCAA CCTCTGGGGA TTCAGTGAGC ACAGCAGGTC GGGGATCTTT 2460
GCAAGAAGCT GCAAGTATTG ACAGAGAAGC TGTAAGCACT CACAGGTCGA GAGCATGGGG 2520
TGTCTCCTGG ATTCTGCCTC TGCTTATGTA GCAAAAATCC CCTGTGCCCC TGCAGAAGGG 2580
TTTTATGCCC TTGAAATCAG GCTGCTACCA TTTTAATAAA ATTTAACCCC TTGATCTTTC 2640
AAGGTGCTTA TATTTTGTAT CCTTTTGGTA TATTACCTTT AGCTTGCCTC TTACTGTTCA 2700
GAGTATTGTT TTGTGACTGA CTCACCTTAG CTCATTTAAT 2740
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