| Tag | Content |
|---|
EnhancerAtlas ID | HS068-03367 |
Organism | Homo sapiens |
Tissue/cell | GM18526 |
Coordinate | chr2:219194030-219195380 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr2:219195217-219195233 | GGTGCACTTTGACCCT | - | 6.58 | | INSM1 | MA0155.1 | chr2:219194432-219194444 | CGCCCCCAGGCA | - | 6.14 | | NR3C1 | MA0113.3 | chr2:219194590-219194607 | TAGAACACTGTGTCCTG | - | 6.02 | | NR3C2 | MA0727.1 | chr2:219194590-219194607 | TAGAACACTGTGTCCTG | - | 6.12 | | NR3C2 | MA0727.1 | chr2:219194590-219194607 | TAGAACACTGTGTCCTG | + | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_13117 | chr2:219194181-219195478 | CD34_Primary_RO01480 | | SE_13701 | chr2:219193625-219196187 | CD34_Primary_RO01536 | | SE_14263 | chr2:219193771-219195977 | CD34_Primary_RO01549 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 219194230 | 219194517 | | chr2 | 219194739 | 219194938 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I218329 | chr2 | 219193787 | 219195999 |
|
Enhancer Sequence | TCAGGGAGCA TGATCGAATC AGGAAGGCCT GGGATTGCGA TGAGCGAGGA GAGAAGGGGA 60
AAGCCACAAG AAACAAACCA AAACTAAACA AAGCCCAGAG CCCTTGGCGG GCAGGTGGCC 120
TGGGATTACA CACATGGAGA CAGAACTAGC CAAGGCCTCC CAGCCAGGGC TGAGACCATG 180
GAGAGGCCAC CAGCTCTTAC TGTGCTTCTG GTCCTAGCCA AGAGCCCTCA GCAGCCCCTC 240
CCCTTCCGTC AGTGACAGAT GGGCGTCCTC TGGAGAGGGC TGTGAAGTCT GGGGAAGAAC 300
CTGTCCTGGG ATGGGCAGGG CGATGGCAGA CCCTGACCTG GGGATCTCCT CTTTTGACCA 360
CGGAGCAGCC CTGTCCCTCT CCTGTGCATG CGGAAGTCCC CACGCCCCCA GGCATGCTGG 420
CAACTTCGGG GAAACCCTTA CCCTCAAGGG CTTTTTAGCT GTTTTGTTAT CTTCTTCAGT 480
TTCCTCAGTT TTGAGAATGC ACAAAACATG GAGCTGCTCT CTGCATTCCT GAGGGGCCTC 540
TAAGCAGACC TCGGGTCCCA TAGAACACTG TGTCCTGGTG GCCCTCCAGG TCCCTCAGCT 600
CTCAGACAGG CACTTTCAGT TCTGTTTCAT TAGGAGTGCC CTGTCGTTGG TGAGATGCAG 660
AGCCTGGGCA GTCTGGGTCC TGAGGACATG AAGGGAGAAA CCAGAACAGT CCCCGGCCAG 720
GCCCCACCAG CCTGAGCTTG CCTGTTGGGT CCCAGTGGAG TCTGGGGCCT TGTGGGATCG 780
GGGGGACATT TAAGGGGTGT AGGAGGAAGG GAGGAGTCAA GGCAGGTGAC CCTGGCAATA 840
GGGGCTTTCC AGATCATTCT GTGGGAGGCA GAGCCCCTGT TATGCTGCTC CCCTGCCTTC 900
CACCCTCCTT CCTACTCCCC CTGGCCTGAG GCCGGCCCTG GGCCTAGCTG GGACAGAGGC 960
TTGAAAACCT TCAGGCTTCT CTCAGGGCTG CCCAGGATGG TGAAATGGCC CCACGGAGGA 1020
GAGAAGAGCT TCATTGTGTG TTTTCCACTG TGTGCCAGAG GGAGGGGCGT CTGGGGGGGC 1080
AGTGGCTCAC TGTCCCCAGC TGTCCCACAT TGCCTCCCAC GGGGCTGGAG GCTCACATTC 1140
AGATACCAGA GACACCAACT GCTGGCTCAC TGAGGCAAGG AGTGGAAGGT GCACTTTGAC 1200
CCTACACTGG AGGTGCTGGT GCTGTCTGCA GCTGTAACCC CACAGGGAGG GTCCCTTGGG 1260
GCAGCTGCCA CTTGCCCAGG CTGGCTGCTC CCCATCTTGC AGAATGGTTT TTCTGCCTCC 1320
CACCTAAGTC CCAGAGGACC AATTGGGAAA 1350
|
