| Tag | Content |
|---|
EnhancerAtlas ID | HS050-05580 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:206747560-206749880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr1:206749069-206749080 | ACAGATAAGGA | - | 6.14 | | REST | MA0138.2 | chr1:206747997-206748018 | TTTGGGACAATGGACAGTGCC | + | 6.23 |
|
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_09327 | chr1:206745188-206758382 | CD14 | | SE_10603 | chr1:206747310-206756416 | CD19_Primary | | SE_11004 | chr1:206727079-206757887 | CD20 | | SE_11917 | chr1:206746090-206750296 | CD3 | | SE_14503 | chr1:206746009-206758997 | CD4_Memory_Primary_7pool | | SE_16490 | chr1:206747976-206750712 | CD4_Naive_Primary_8pool | | SE_16959 | chr1:206747363-206748061 | CD4p_CD225int_CD127p_Tmem | | SE_16959 | chr1:206748089-206757504 | CD4p_CD225int_CD127p_Tmem | | SE_17411 | chr1:206724289-206760065 | CD4p_CD25-_CD45RAp_Naive | | SE_17843 | chr1:206723887-206758306 | CD4p_CD25-_CD45ROp_Memory | | SE_18269 | chr1:206723684-206769868 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19128 | chr1:206746389-206766399 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20034 | chr1:206746357-206757932 | CD56 | | SE_20823 | chr1:206746904-206757454 | CD8_Memory_7pool | | SE_22080 | chr1:206746077-206757652 | CD8_Naive_8pool | | SE_22390 | chr1:206744356-206757869 | CD8_primiary | | SE_25703 | chr1:206746359-206750220 | DND41 | | SE_27304 | chr1:206748233-206749980 | Esophagus | | SE_31229 | chr1:206747597-206750097 | Fetal_Thymus | | SE_39708 | chr1:206748495-206749981 | Jurkat | | SE_50667 | chr1:206747343-206754765 | Sigmoid_Colon | | SE_53261 | chr1:206746644-206756568 | Small_Intestine | | SE_53552 | chr1:206746429-206757806 | Spleen | | SE_55221 | chr1:206747302-206748199 | Thymus | | SE_55221 | chr1:206748265-206748685 | Thymus | | SE_55221 | chr1:206748689-206750305 | Thymus | | SE_59167 | chr1:206727342-206757447 | Ly3 | | SE_62534 | chr1:206724532-206763666 | Tonsil | | SE_65624 | chr1:206747328-206748146 | Pancreatic_islets | | SE_65624 | chr1:206748409-206749787 | Pancreatic_islets | | SE_66615 | chr1:206748495-206749981 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 206748926 | 206749451 | | chr1 | 206748515 | 206748888 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I206573 | chr1 | 206746529 | 206757654 |
|
Enhancer Sequence | GGGAGTGGCC TGATCTGTGC TGCTTGAGGC TTTTTGTCCC AGATCACACT GTACTTGCTC 60
TGGTGTGCCA CAGCGCATCC ATCTCTGTCT TCCCTTCTCA GGTCACCTGC AGACTCCCAA 120
GGACAGGGTC ACATCCCATC TGCGTCATCT CTCAAGGTGC CTTTCACGAT CCTCACCCAT 180
AGGCAGTTCA TTCAGTTACT ACTGGCGGAC TGTTGACATT GACCATCTGC TCTACGTTTT 240
TGTCTTTGGA GACTTGAGTC TCTTTCCATT CTCAACCTCC ACCCGCCACC TCTTTTTTCC 300
CTCTGCTCTG TTAATACACC CTACCAGAGC TGCTCAAATT CCACATGGAG CAGAAGCTCC 360
ATGATAAAGC CCCTTCCCTG CTCTGCTGCA AATAACCTAT TAGGGAACAC AGTTAAGGAG 420
TTCCCAACCC TTTTAATTTT GGGACAATGG ACAGTGCCAT AGAGGGACCT GTGGAAATCA 480
ACCCCTTCAC TGCTGTGGTG GGTCTGTGGA GTCCATTTCA GAACACAGGC CTTCGAAGAC 540
CTGGGAGGGG GCCCTGCAGT AAGGCCCCAT AGGGATTCCT CTTTCTCATT TGGTTGAGAC 600
CATCACAAAG GGACCAATGA CTTTTTTTTT TTTTTTTTTT TTTTGAGATG GAGTCTCGCT 660
CTGTCATCCA GGCTGGAGTG CAGTGGCGCA ATCTTGGCTC AATGCAACCT CTGCCTCCCA 720
GGTTCAAGCG ATTCTTCCGC CTTAGCCTCC CGAGTAGTTG GGATTACAGG CGCACGGATA 780
ATTTTTTTGT TTTTGTTTTT GTTTTTTTTT TTAGAAGAGA CAGGGTTTCA TTATGTTGCC 840
CAGGCTGGTC TTGAACTCCT AACCTCACCT TTGAATGCGG TTTGGACATT GAGCAGGGTA 900
TTTCAAATCC AGCCCAGATA GATGGGTGTC TGCCCCTTGC CTGCAGACGT TCCCATCTAG 960
GGCAAGCACA ACAGAAGCAC CGGGTGTTTG GGGTGTGGAA GGCAGCTGCA GATGGACATT 1020
CTCCTGTAGG AGGGGCCTGA GGCTTTCCTC CCTGACTTAA GCCTGGAGAT GGCTTCCTTC 1080
CAAGGGGTGA AAGAATTGCT GCTGACAGAT TTGCTAAGAG CTGAGAAAGA GGAAATGTGG 1140
CAAAGGCTCA TGGTGAATGG CTTCCGGGGT ATTTTTTGTT TTGTTTTCTT GAGTTGTGTG 1200
TGTTAAGAAT GCGTAGACCG GCTTGGGCTT GGCTAAGATA GAGTCTTGCT GACAATAGAG 1260
AAAAGTGGTG AGCAGTGAAA AAGTAAAGTC GTGGCGGTTA GAAATGTTCT TTGTGCTCCT 1320
TTAGATTGGT TATTCCTGCT GCCATTCAGC CATGCTAGCT AGCCTCCAAG AGGCCCCCAT 1380
CTCCACACCC AATTCTCTGA AATAGAAGAG GAAGCAATGA TGAGAAAAAA ACACCACCCT 1440
ATCTTATGTG TAAAATCTTA GTCCTGCGAA GGGGCCCTTA GAGCTTCTCC AGTATCACTT 1500
CATGATTTCA CAGATAAGGA AACTGAGGCC CTGAGAGGGG AAGTAGCTCC CCAGACGTCA 1560
CAGGTCATTT GATGGTCTTG CATTTGTTCT CATCAGCTAG CTGCCAAGAG CTGAGCCACA 1620
CGGCTAACGC CAAAGTCCAA AGCCTGGTGT GTGTTCTTGG TATCAGACCC TCAGGGTGCA 1680
GCTGAGTGTG AGGTGCTCCT GGACCTAGGG GTCTGGGGTG GGCTCTGGCC TGAGACTCCC 1740
CAGGCTGTCT TGCCCTCCCC TGCCACCCAA TCAACAGGTA TTTATCTGAC ACCTACTTAA 1800
AGTTTGGCCC AGGTTTCAGC CAAGCGGGGT GCCAAAAAGC TTAGGCACCA AACTAATGTC 1860
TGCCTCCATC CAGAGAGCAT CTCACTGGGG AGATGGGATT AACATGTGAA ACAATCATTA 1920
AACAATAAAA GGCAGCATAT AATTAGATGC CAGCTGTAGC CACACAGGCT CTGAAATCAC 1980
CTCTATAGGC TCTTGCAGTA TGGATTTAAC ATTAGCCAGC AGCTGCAGAG ATCTGTGACG 2040
ATGGTAATTT GTACTTTTGC TGCAATGGGA ATCTGAGGCT TTGAGGCCAT GGGGCTGGTG 2100
TTTGGGAGCG AGTCACAGAA CCAGGGAGTG AGCCTAGCTG TCTACCTCCA TCCCTACCCC 2160
AGCCAGCTTT GTTGCCTCCT CATTGCAGAA TGGAGTAAAG TGAGCAAAAT CCAAGGAAGT 2220
GCCCAAGCCT TTGTCTTCTT GTGAAAAGTG TCCATGAAAT GAGAGTGAAG TTACAAAGGC 2280
CCATTAACTG GTGGTGTGAG GAAATACACA GGAAACATAG 2320
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