Tag | Content |
---|
EnhancerAtlas ID | HS102-12940 | Organism | Homo sapiens | Tissue/cell | HuCCT1 | Coordinate | chr2:97330080-97332420 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr2:97330587-97330598 | TTCTTATCTTC | + | 6.02 | TFAP4 | MA0691.1 | chr2:97330789-97330799 | ATCAGCTGTT | - | 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 |
GH02I096664 | chr2 | 97330129 | 97332421 |
| Enhancer Sequence | ATTCCACCCC CTCCCATCCC CAGGCAACCA ACAATCTGCT TTCTGTTACT ACGTATTAGC 60 TTGCATTTCC TAGTGTTTCA TAGAAATGGA ATCGTTCAGT AAGTACCCTT ATTTGTCTGA 120 CTTCTTTCAC TCAGCATAAT TATTGTGAAA TTCATTCATG CCATTGCTGT GTATCAGTGG 180 TTTATTCCTT TTTGTTGCTA AGTAATATTC CATTGTATGG ATGTACCACA GTTTGCTTAT 240 CCCTTTCCTT GTTTATGAAC ATTTCCGGTT TGGGGCTGTT ACAATGAAGC TGTAAACACT 300 TGTGTACAAC CCTTAGCATA GACATATGCT TTCATTTCTC TTAGGTAAAT ATGTAGATGC 360 AGAATGACTA GATTCTATGG TAGATGTATT AAGCAATGAG TGGGTCATAC AACTGAACTT 420 TCCAGAGAAC TTAAATGTGC CCTTTCACCC ACATATAAAA ACAAAACAAA TCCCTTTAAA 480 GACACATTTT AAATGATAAT ATACATTTTC TTATCTTCTC AGCAACTTTG CCCTGAATAT 540 AATTAGAGCT TTTTGTTGAT GGCCTGGAGC CATTATGGGA ACATAGTTAT TATCCTGGGC 600 TATCTGCAGT ACCGGGCTAC TTGTTCCTGC ACTAAATGGC TCTGAGATGC TTTCTTTTTG 660 GGGTTCTGTA GTCTGATTTT GATCGCCTTT CAATCTGTCT CCGTCACCTA TCAGCTGTTG 720 TGGATGACAG TTCTCTTGAA GGCGGAGTCT TACTGGCCTT TTGACTCTAA GTCAGGCTTC 780 TAAGAGCAGT GTGTAAAATA AGAACACAGT TCTGAGAGAG AACTTGAGCT GAGAGATAAC 840 TTGAGCTCTC TCATAAGTGC AGGCACACAG GAATTTGTGT GACATGGACT TGGCAACCCA 900 GAGAATGTTT TGTTTCCTCA TACCTTACAT TGTGAAATAC AAAATTAGCT AATGCGCTCC 960 CCTTCTCCCT CCTGTGAACT CCCCTCCTTG CTGCTTCTAG TAGCTACCCA GTCTGCCTTC 1020 CTGTGAGTCA TCACTTTCAA CCATTCCTCA TAATCCCTGC CTCCTTGGAT GATTTTATAG 1080 ACTCTGAAAG TAGGAAGACA TTTCAGAGGA GGCCTAGTCC ATCCCCCATC CTTGCCAAGC 1140 TCCCTCCCAC CTTTTCCGGC CTGTGATGAG GGCACAGGGC TGGGATCCTC AGATGTTCTG 1200 TGGCTGTTCA GAGCCTTGGG AAATCTTCTT TTTTCATCTT CTGTTCATCT TCTTTGTTCA 1260 TCTTTTTTTT TTTTTTCTGA GACAGAGTTT CATTCTTGTC ACCCAGGCTG GAGTGCAATG 1320 GCGCGATCTC GGCTCACTGC AACTTCTGCC TCCTGGGTTT AAGCTATGAG TAGCTGGGGC 1380 TACAGGTGCC TACCACCAAG CCTGGCTAAT TTTCATATTT TTAGTAGAGA CGAGGTTTCA 1440 CCATGTTGGC CAGGCTGGTC TCGAACACCT GACCTCAGGT GATCCACCTG CCTTGGCCTC 1500 CTACAGTGCT GGGATTACAG GTGTGAGCCA CCATGCCCGG CCCTGTTCAT CTTCTTACAG 1560 GCTCAGAACC AATGGCACAG GCCAGGCCCT CCCTCATCCC TGAGAGAGGC CTTCCAACAT 1620 TTGAAGATGT TCAAACACCC CTGGAACCTC ATCCATTTTC CCCAGAACAC AGTCTCCAGG 1680 GTGGGGCCCT TTGGATACTG GCCTGATTGC CTTTAGCCCT TTGGAAATGC AGCAGGCAGG 1740 TGTGAACCTC TCTCTGAAGA GGCAGAACAG CCAGCCACAC AGATGGCAGC ATCTGAGGCC 1800 AGGTGGTCAG AAGGGGAGCA GAGCCCAGGG CACTGCAGAA AACTGGCCTG TACCAATGGT 1860 CAGTCCGAGG GCCCCAGGGC AGAAGGGGAG GCAGCACACT AGATGAGGAA CCAAGAAGCA 1920 GGAGGAGAAT TATTAGCAGG ATGGATGGAA AGGTGGTTCC GCCATAAATC TGAACTTGGA 1980 GGACTCCTAA CTTTGGAAGA CCTGGATGCC TTCTGGTGCC GATCTCTCCC CTTCCAATGT 2040 CCTTCCTTAA CCTGGGCAAT TTCCTCCTTT CTTACTGACT AGCTGCTCAC CTGGAAAGCC 2100 CTTTCCTCTT CTCCTTGGCC CCTTAGCTGT CAGGACCCAG GGAGAATGGG ATGAAGAAAA 2160 TGGAAAGCTG GGAGGTTCCC AGCCACATCC CAAGAACTGC TGTAAGGAGA AGAGGCCCCA 2220 GCTGAGAGGA TTGAGGATTT GGGGTCCCAC TCTGGCCTCA ACCCAGCAGC TCTATTTTAC 2280 ACATGGACAC ATGGATTTTT TTCTTTTATT TATTTATTTT TTTTTTTTAG ACAGTCTTGC 2340
|
| |
|
|
|