| Tag | Content |
|---|
EnhancerAtlas ID | HS038-11772 | Organism | Homo sapiens | Tissue/cell | ESC_neuron | Coordinate | chr2:130860010-130861200 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr2:130860163-130860180 | AAGGTCGTGGTGACCCT | + | 6.29 | | ESR1 | MA0112.3 | chr2:130860163-130860180 | AAGGTCGTGGTGACCCT | - | 7.14 | | ESR2 | MA0258.2 | chr2:130860164-130860179 | AGGTCGTGGTGACCC | - | 6.06 | | IRF1 | MA0050.2 | chr2:130860650-130860671 | ATTTATTTTCATTTTTCTTTC | + | 6.05 | | IRF1 | MA0050.2 | chr2:130860665-130860686 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | Nr2f6(var.2) | MA0728.1 | chr2:130860892-130860907 | TGATCTTTTGACCTT | - | 7.24 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAGAAGCATC TAAGGTAACA CAGTATGTTG TTCTCCACTT CCTAATAGTG AAGCAGTAAA 60
TGTAAAGAAA AGGAAATTTA GTTTTAAAGA GAAACAAGTT TTCCCGCACT TAGCTAGTCT 120
GACTCTAAGG ATAGTAACAA GCAGGGCCCA GGAAAGGTCG TGGTGACCCT GCCTGAGAAG 180
CCAGAGCCCA CAGGTATGGG CTCCAGACAT CCCAGAGCAA GGTTAAGAAA ACAAAATCCT 240
TTACTGTCTC CCCTTCCCCT CAGCATTCAC TCAGAGCTGT TTTTACAAAT GCATACTATT 300
CGCAAGTTCC TGTTGACCTT CAATGCAGCT GCAAGGTCAT AAGCTTTGCT GAGGTTGCAA 360
AACTGTCACT ATATGATTAA CTGCCTTTGT TCTGCTTCTG TAAGCTTGCC TACATAAGCC 420
AAGCCCTGTC TTTGTTCAGG GCTCAGCTTT CGGATGCAAA TCTGCTGAGC TGTTGCGAAC 480
CTAAATGAAA TCCTCCTGTT TCACCCACTT GGTCTCTCCT GCCTCCTGCT TTCTGCAACA 540
ATAGTACCTT ACAAATGATT TCAAAAATTA CTACTGACAC CTTTATTAGT GTACAATGTC 600
TTCCCAATAT CTAAAATGTT TTCCTCCACT ATTCTGACAC ATTTATTTTC ATTTTTCTTT 660
CTTTCTTTTT TTTTTTTTTT TTGAGCCAGG GTCTTGCTCT GTCACCAGGC TGGAGTGCAG 720
TGGCGCAATC TCAGCTCACT GCAACCTCTG ACACTCCCTG GTTCAAGCGA TTCTCCTGTC 780
TCAGTCTCCG GAGAAGCTGG GATTACAGGC ATGTACCATC ATGCCCAGCT AATTTTCGTG 840
TTTTTAGTAG AGACGGGGTT TCACCATTGG CCATGATGGT CCTGATCTTT TGACCTTGTG 900
ATCTGCCTGC TCCAGCCTCC CAAAATGCTG GGATTAGAGG TGTGAGCCAC CACACTTGTC 960
CTTATATTTA TCTTTTAAAA CAATGCTATG AGAACGTCTT CCTTGATTCT GCATGTCTTT 1020
CCCCAGATAA ACAGGTACCT CCTTCCTTGA GGCTGCCTTA GTACTTCACT GATTTTTCTA 1080
CTGCATCTTT ACCACCTGAA CTGTACATTA TTCCTCCACA TGTCTGTCCC GTCTGCTCCA 1140
AGACTGCAGA GGACAGTCTT GAGCATCATC TTACTCACAT TTTACTCAGA 1190
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