Tag | Content |
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EnhancerAtlas ID | HS141-05399 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr13:96359790-96361480 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr13:96359927-96359941 | AGAAAGGGGAAGTT | + | 6.43 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 96360073 | 96360204 | chr13 | 96360212 | 96360600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I095707 | chr13 | 96359423 | 96361054 |
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Enhancer Sequence | TGCACTGAAG CCCAAGGCCA TGACCAAACC AGTCCTCGAA TTGCATCTCT GTGGGCCTGT 60 CTCCTAGGAC TGCTCCCAAT ACCAATTGTG TGTCACTCAT GGTCCGTTGA GGAGAGACCG 120 AAATCATGTA GTTACTTAGA AAGGGGAAGT TTAATCTAAG AACTGTTAAG TTGTGATAGG 180 AGAGTAACTA AAGATGTAAA GAGAACTCTA ACGGATATTC TAGGACTAAG AGCCTCAAGG 240 AAGGACCAAC TTGCAAGAGG GGTCCCCTCT ACCAGGCTGG GGTTTAGAGC TTATTGGAGA 300 AGGTATAGCT GTAGCCCAGG TTTGCTGGTG GAGAAGATTG CTGTGTGGCT GGTCCATAGT 360 AATTGGGCAA GCAGGAAACA ATCCTTTCAT GTATAGGTGA GCGAAGGCTG GTTAGCCTGT 420 CTACGAAGGG AGTCCAGGTG CTTCTGTGGG TGTGAAATCT GGAGTGTGTG GGCTGAGGTT 480 GCCAGATCAC TGAGGAACTG GACCCCTGGG CATAAGCTGT GGCTAAGTAC CCCTGGATGT 540 CCTCCTCATC CATACCATGC AGCAGGAAGT CCACCCCATG ACAGACCATG CAGCAGGAGC 600 CAGAAGACAG TAAAATGCAC CAAGCAGAAC TAGGAAGTGT CCTTTCTGCA GTGTTGCTTC 660 AGTGCCCTGT ACTGACAAAG CATAACATTG TACTCACTGT AAAGAGGAAA TGCCTGCAAA 720 CTCCAGGCCT TTATTGCAGT GCAGGTACCG AAGGATGAAT TCAGAGCGGA GAGGCAACAT 780 ATTGATAATT GGCCTAGTCC ATCAGATCAT GTTATTGATT CCACAGTAGT TCCCTGTTTT 840 AAGACAAGTA AATATTCAAA GCTGTAGACA GGTCCTCTAC TTCTTTGACC TCATACTACT 900 ATCTTCCTCT TGGCTCTGCT GCAGCCATCC AGGCCTTTCT CCTGTTTCTG GAACATATCT 960 GCATGCTCCC GACTTAGGAC CCTTGCTGGT CCCTCTTCCT GGAAGCTATT TTCCTAGCTG 1020 TCTGCATGGT GAGTTCCTCA TTTTTTTCAA GTCTTGCTCA GATGTCAGTT TCTCAAGAAG 1080 GCCTGCCCTT TACGCGCTTA TTTGCTACTC TAAGTCCCCT GAACTCCTTA CCTCTTCACA 1140 TGGCTTGACT TTTTCCACAG TACTTTTCAC CCAACATACT ATATAATTTA CTTATTTATC 1200 ATGTCTGTCT CCTCCCACGA TAACATCAGG CGCCAGGACG GTATGAGGGG CAGGAGTTTT 1260 TTAATGTTGC TCACTTATTG CAGATACCTA AAATAGTGCC TAGTGCATTA TAGGTGCTTA 1320 ATAAATACTT AAATATTGTA ACAGTCTCTA TGATGTTCAT TAAAGGTGAG ATTCTACCTT 1380 CAAACAATTT TCATTTTATT ATTCAAAATA TTTTTACTAC TTCTGCATTA CACAACTTCC 1440 CTTTATTTTC TGGACTGGTT ACATTCTTTT GACTGATTAG GTCAAGATGG GTACATTTTT 1500 TGTCTTGTGC TCCATATAAT GAAATAGGGT TTGTATTTTA TGTTACGTTC TTTACATCAT 1560 TTTTCAGCTT CTGTGACTTT TCTCATCTGA GTAGATGACT GAGACAGATA ACTATTTTTA 1620 ATATTATATT TTTTAGAATT AAATCTTAGT TCGTGGAAAG TTAACTGATT GTTTTTAATT 1680 TTATTTTTAG 1690
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