| Tag | Content |
|---|
EnhancerAtlas ID | HS020-24832 | Organism | Homo sapiens | Tissue/cell | CD34+ | Coordinate | chr2:86238260-86239780 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr2:86238360-86238371 | TTTCCCAGAAG | - | 6.62 | | TCF7L2 | MA0523.1 | chr2:86239421-86239435 | TGTCTTTGATCTTC | - | 6.41 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 86239255 | 86239427 | | chr2 | 86238946 | 86239215 |
| Enhancer Sequence | TAGGTCAGCC CTCTGCCAAT CTCTAGGCAT GCCAGTGGCA GCAAGGTGAC TGCCAAGGGA 60
AGAAGGGGAT GGACCTCTCC CTATGGATGT AACTAGGTAT TTTCCCAGAA GCTACTTACA 120
TGCCATTGAT AAGGGTCTGG CCAGTCAAGA GCACAGGGGC TGGGGTTGCT ATGATTGGTT 180
TAGGCCACTT ATAGCTGAAC ATATTACAGC CTGATTGAAA CTGGGGTTTT GTCAGTAGGG 240
GAGGCAGAGC AGGCAGAGGG GCTGCAAAGT AGGGAGTGAG ATGTCAGACA ACTGCCTTTG 300
CTGCCTCCCC CTAGTCCCCA TTCTGGGAGC CCACTGTAGA AGACACAGCG GGCGGTAGGA 360
AACATATGTG AAAAAGCTCG ATTTTTACAA TGCAATAAAC ATTAAACAGC TTTGTTGGAG 420
AGCAAGGAGC CTCATAAAGT GAGTCACCCA GGATCCTTCT CGCAGGACTG GGGCATGCCA 480
AAGAGCAGGC TTTGAGTGTA GGTAGACCTG GCCGCCTCTC AGTGCACCTC TGATGGCACC 540
AGCTCCTGGG CAGGGAGCTG TTCCCCCAGG GCACTGGCAT CTGGGCAGGG CCAAGGAAGT 600
CCTCACCTCT GTGACTCTGC TCCCAGGCAC TCGACATCCT TCTTGGCTGG GAAAGTGTGA 660
CCTCCAGGAA AATGCTGGGG ACGTGCAGAG GCCAGCGCCC TCTGCATGGG TCTCCTGGGA 720
GGCCTGTGAG GGGCCTGGGA AATGATCACA GGCTTTTCCC AGCCTTCCTT CATCCTTGGG 780
AAATTCGCTG AAGGCCAGTC CCCTGTTGAG TGTGGGGCTC TAGGCCCTCT TGGGTCCTGA 840
GCAGAGCTGG GCCCCACTCC TTTCTCTCCC AGCAGTGACC GTAAGACACT GCCCCCAAGT 900
GAGGAGAGGG ACCCCTGTGT GAACCGGCTG CAGGAAGCCC TTGCTCCTTT CTCAAGGCTG 960
CGAGCCAAAG AGAGCAGGCT CCTGGGGCTG TCTCTTCACT ATCCAGTCCA GCCCTAACAA 1020
CCTACTCCTG CTTGGGTCTC CCCGCCCCCT ACCCTCTGCC CTGTGCTCCC ACCATCCACT 1080
TCAGGCGAAA GGGAGAGTGT GCTGTCCTGT ACATGCTCAC ACATTCCTGT GCCTATTACC 1140
TGGCCCCTCA CCTGGAAGGC CTGTCTTTGA TCTTCCACCT AGACAGAGTT GCCCCCCTCT 1200
GGCCCTCCCA ACATGCAGCT GACCCAGGAT GGTCCTGCAG CCCACAATGG CCTCGATGAG 1260
CACATCTCAC AGGGCTAGGT AGGGGGCACT GGCAGAAAAT TAGCACCCAA TGGGGAGAGG 1320
CTGCAGCAGG ACCAGAGCAG GAGCATGGCC AGGGCAGGAT GCCCACCTGC AGCCGTCCCC 1380
AGGGGGCTTG GCCATGTGGC ATGCGCTGCT GGTGGAGGAA GCTTGGCTGA GCATGGGGGC 1440
AGGGGAACAG GCCCCCACAC ACACTCAGAT GCACGTTTAC AATCACATGA GCTGCATTCT 1500
AACAGCTAGT GTATGTCCTT 1520
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