| Tag | Content |
|---|
EnhancerAtlas ID | HS092-24660 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:127840470-127843230 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr2:127842205-127842216 | AGAGATAAGAA | - | 6.32 | | Gata1 | MA0035.3 | chr2:127842205-127842216 | AGAGATAAGAA | - | 6.32 | | KLF5 | MA0599.1 | chr2:127842613-127842623 | GCCCCGCCCC | + | 6.02 |
|
| | Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
| SE_00572 | chr2:127838207-127846198 | Adipose_Nuclei | | SE_00914 | chr2:127837091-127843980 | Adrenal_Gland | | SE_03157 | chr2:127840812-127842608 | Brain_Angular_Gyrus | | SE_03157 | chr2:127842878-127844118 | Brain_Angular_Gyrus | | SE_03883 | chr2:127821506-127844236 | Brain_Anterior_Caudate | | SE_04777 | chr2:127820278-127857314 | Brain_Cingulate_Gyrus | | SE_05775 | chr2:127806116-127867885 | Brain_Hippocampus_Middle | | SE_06689 | chr2:127821297-127857092 | Brain_Hippocampus_Middle_150 | | SE_07740 | chr2:127821073-127849400 | Brain_Inferior_Temporal_Lobe | | SE_08942 | chr2:127842192-127842509 | Brain_Mid_Frontal_Lobe | | SE_19824 | chr2:127842348-127843293 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_22831 | chr2:127831598-127840986 | CD8_primiary | | SE_22831 | chr2:127841008-127845265 | CD8_primiary | | SE_24390 | chr2:127841733-127843718 | Colon_Crypt_2 | | SE_29563 | chr2:127836160-127857245 | Fetal_Muscle | | SE_31713 | chr2:127837676-127844066 | Gastric | | SE_36991 | chr2:127828440-127865759 | HSMMtube | | SE_41757 | chr2:127841273-127843893 | LNCaP | | SE_48048 | chr2:127806769-127857236 | Psoas_Muscle | | SE_50749 | chr2:127840740-127843883 | Sigmoid_Colon | | SE_51095 | chr2:127817891-127857315 | Skeletal_Muscle | | SE_54239 | chr2:127840923-127843925 | Spleen |
|
| | 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 |
| GH02I127071 | chr2 | 127828680 | 127857094 |
|
Enhancer Sequence | AGGGAGGAAA AGAGGTTCTA AGCCCACCAC TCACCTCCAC ATTTCATGTG GCCCTCTCAC 60
CTCCTTATTT TCAAAGTATA AACCTCAAAG AAAGTGGAAA GGATACTACA GGGACTATCA 120
TCTACCCTTC ACCCAGATTC ACCAATCAAC TGTTACCACT TGGCCACACT CATTTGCTTT 180
TTTCTTTTTT TTTTTTTCTT TTTTTTTGCT TTTCTCTTTT CTTGCTATGT CGTCCAAGCT 240
AGAGTACATG GCGCAATCAT GGCTCACAGT AGCCTAGACT TTCTGAGCTT AAACGATCCG 300
CCCACCTCAG CGTCCCGAGT AGCTGGGACT ACAGGCCACT GCACCTAGCT AGTATTTTTA 360
CTTTTTGTAG AGACAGGGCC TCGCTATGTT GCCCAGTTTT GTCTGGAACT CCTAGCCTCA 420
AGTGATCCTC CCACCTCAGC ACCCTCAAGG TGCTGGGATT GCAGGTACAA GCCACCGTGC 480
CCAGTCACTT TTCTCTATAT ATAAACCGTT CCTGCATTTG TATGTTTGCC CAGCCAACAG 540
AAGGTAAGCA GCAGAAGGGT CACTGGGATG ACCTTCGCTC CACAATACTT CACCCCTAAA 600
TACTCCAACA GATTTCCTAA GAACAAGAAC ATGCTCCAAA ATGCCCATGA TACCATAAGC 660
ACCCCCAATA CATCCAAAAT GTATTTTAAA ATACCATCTA CCACACGGTC CGCATTCAAA 720
TATCCTTGGG TGCCCCCCAA ATGCCCTTTA TGTCTGGGTC TAGGATCCAA CTGTGGTTCA 780
CATATTGCTT CTGATTGTCG GGTCTCTTGT TCCTTTAGTC CAGAATATTC CCCGTATGCC 840
TATTTATCAA TGTTATCCAT TTTTTTTCTT TCGTGATACT GGTATCTTTT TAAGAGTGCA 900
AACCAATCAC TTGGAGAATG CCCCACACTC TGGATCCATC TGATTGTTTC CTTGTGAGGA 960
AGTTCAGGTT AAAGGCTGCT TTGGCAAGAG TCCTGCAGAG GGAGGCTGAG CCTTCCCACC 1020
GCACCACAGC TGTGTTAGGC TTGACCGCCG GGTCTGAGTC GTGTTTGCCA GATCTCTTGG 1080
AAAGGAAGGT CACTTTTCTC TTAGTCATCT GCAGGACAAT CACGGTCACT GTGGCAAGGC 1140
AAAAAGTTGT TGAAATTTTT GCACAGTGCC TTTACTATCC ATCATTCTTT GCTATTCAGT 1200
GTGAGGTCTG TGGGCAGCTG CATGACAGTC TTCCAAGAGC CTGGAGGAGA AAAAAAACTG 1260
CAGACCTGCT GAACCAGAGT GTTCCCTTTA ACAAGTCCCC CTGGCGCACC GTATGCGCAG 1320
TGAAGTCTGA GAAGCACTGC AATAGCATCT TGGCTGGAAC CCGCTGTTAC CCAATCTCCT 1380
CCACGTGACC CGGCATTCCA CAAACACGAG CCTCCCCTGG TCTTGCCTTT GCGAGGAGGG 1440
TGGTGAGGAT ATCGTGAGTC CTTCGTTTTG CGTTCGTGAT TCATTTTGAT GCTCAAACAT 1500
CCCAAGTGCG ACCAGTGGGA GGTTTCGGAC ACGTCCTCAT TCATCTCCAG GCGCTTCCTT 1560
ACTTTCTGGC ACTAGCAGAT TCTCCAGGCT CAGCCTGCAC TGTCCCTGCC CCAGCCCTGG 1620
CATCAGCCAT TTCTCCAAGG AACCCTGATT TCCTTCGGTG GAGAGGCATG CTCATTGCTC 1680
TTAGGCATTT CAGCGTTCCC TCATGCTCAG AGCCGCAGAT TATTACCCCT GCTTTAGAGA 1740
TAAGAAAGGA AAGGCTGCGG CACTGAAGGA TTTGGCTCTG CAGCGAAGAA GCGACCGAGC 1800
TCAGATTCTG TGGCTTTGTG GTGGTGGTGA ACAAGCATCA TCACTCAGGT CTGTCTGCTT 1860
CAAGAAGTGA GAAAGGAGAC AGACCCATGG CCTAGCAGCT GCCCTCTGAG CCCATTGCAG 1920
TGTTCCTTAG GAGGCCACAC TGACTGTGGG CTGTGGCACC TGCCCCAGGC TGGTGACTGC 1980
ACAAGGGGCA GCTTCCTGGT CTCATCCAGC CCAGGGAAAC TCTCTTCCTC CTCAGAACCC 2040
AGTGAAGTCA CACGTACAGA GGCGTCTTCA GAGCAGCAGT GCTTAACCCA GAAGCTAGCA 2100
GTCTCCTGGT GACGATTGAG GCCTTGTTCT CCCTCCATCC CCCGCCCCGC CCCACCCCAG 2160
AGCTGCTGCT TCACCCTCAG GTTGGGAGGG GAGGGCACCC AGACCTGCAG CCAAGGACAG 2220
AGGGGCTAGA ATGAGGGTCC CAGACTCCTT GGGAAAGCTA CGGGCAGCTG GGCCCCTTGC 2280
AGCAGCCCCA GCTGTGGCTG CAAAGGGGAG AAGTGGCCCA GGTTCCTGCT GGAGAGCAGA 2340
GCCCAGGGGC ACCGGGAAGT GAGTCCCAGG AAGCAAGCCC AGAACACACA GCACACTTCT 2400
TAGCGGCTAG CCACCCTTCA GGCTATGCCT TCCAACTTCT CAAAGGCACA ATGACTTTAA 2460
AGATAAGTGC ATTCCATCTG GAGGCAAGAA CGCTCCCCAG CCCTCAGGGC CCCACACAGC 2520
AGCACAAGCT CGGCCATGTA CATGCAGCAA GCACCTCCAG TGTGAGATGA CGCCCACACA 2580
CGCTCACACA CACCCTCCCT GGCAGAGCCA CCTGTTCATG GCCCTCCTGG GCACAGTAGG 2640
AAAGTGGAGG AACCACGAAG AAGCCACAGA GACAAGCAAG AGGCAGAGGG AGGCCCGGGG 2700
AGAGCCCATA ATGAGGAAGG AGCCCGAAAG AAAACCAGAG ATGGGGAAAC CAAGAGCGAG 2760
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