| Tag | Content |
|---|
EnhancerAtlas ID | HS034-13136 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr17:71287150-71288950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr17:71288636-71288656 | TGTGGGGGGTGGGGGTGGGG | - | 6.17 |
|
| | Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
| SE_00203 | chr17:71281786-71292211 | Adipose_Nuclei | | SE_00919 | chr17:71280759-71290474 | Adrenal_Gland | | SE_01949 | chr17:71286022-71290366 | Aorta | | SE_02957 | chr17:71286918-71287765 | Bladder | | SE_02957 | chr17:71287829-71289133 | Bladder | | SE_04533 | chr17:71284556-71288674 | Brain_Anterior_Caudate | | SE_06356 | chr17:71277769-71290798 | Brain_Hippocampus_Middle | | SE_23373 | chr17:71285973-71289030 | Colon_Crypt_1 | | SE_23953 | chr17:71286005-71288922 | Colon_Crypt_2 | | SE_24951 | chr17:71286071-71288667 | Colon_Crypt_3 | | SE_26142 | chr17:71284616-71290403 | Duodenum_Smooth_Muscle | | SE_26892 | chr17:71286041-71290403 | Esophagus | | SE_28228 | chr17:71284304-71287350 | Fetal_Intestine | | SE_28228 | chr17:71287427-71288323 | Fetal_Intestine | | SE_31497 | chr17:71284450-71290426 | Gastric | | SE_34366 | chr17:71286076-71290834 | HCT-116 | | SE_34727 | chr17:71283787-71290955 | HeLa | | SE_40779 | chr17:71281080-71291827 | Left_Ventricle | | SE_41738 | chr17:71286058-71288619 | LNCaP | | SE_42276 | chr17:71282392-71290554 | Lung | | SE_44396 | chr17:71285868-71289101 | NHDF-Ad | | SE_45062 | chr17:71286886-71289026 | NHLF | | SE_46731 | chr17:71286991-71288670 | Ovary | | SE_46731 | chr17:71288712-71288904 | Ovary | | SE_47498 | chr17:71286740-71289028 | Pancreas | | SE_48667 | chr17:71282058-71290313 | Right_Atrium | | SE_49576 | chr17:71286813-71289033 | Right_Ventricle | | SE_50297 | chr17:71283561-71288835 | Sigmoid_Colon | | SE_52570 | chr17:71282759-71290321 | Small_Intestine | | SE_53786 | chr17:71283801-71289650 | Spleen | | SE_54836 | chr17:71279223-71290708 | Stomach_Smooth_Muscle | | SE_57720 | chr17:71287754-71288504 | VACO_503 | | SE_65340 | chr17:71280793-71290305 | Pancreatic_islets |
|
| | 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 |
| GH17I073287 | chr17 | 71284034 | 71291744 |
|
Enhancer Sequence | CATCCTTGCG GGTAGAACTA TTGAGGTAGG TCAGAGGGGA CAGCAGGGAA ACTCAGCTGA 60
AATCACGGCC ATCCTGGGCT AGCCCTGGGG TCCCCAGGAT CTTGTTCAAC CCCACACCCC 120
AGAAAGACAG GGACAGGTCT ACCCAGTGCT GCCTGCTGCC ACGGTCTCGC TTCCTGGGGG 180
GTTGGGAACG AGACTTTGTG GCTTGTAGAA AGCCATCTTC AATAACCAGC AAGGAAGGGT 240
CCTGAGAGAG TTGGGGCCTA GAGGGAGTCA CGCATCTGTC CCACTGCCCC AGCGAGGAGG 300
GGGCTGCAGT ACCTGGCAGT CCACACTGGG GATGAGGCCT GGGTGTCTGG AGCTCAGACT 360
AGACAGGCCA CCCAGCAGGA TTGAGGGTCA GCAACAGCTT GGTTTCACCA GCCTTGAGTG 420
ACCTTGAGTC ACTCTGAGCT TCTAACAGAG AACAGTTTGG AGGTGACGAG CTGGATCATA 480
GAGTTTAAGA GAAAGTAGGT GGTGGGAGTC TCGCCAGAGG CCTGGGCAGG TCCTGGGGGC 540
AGCTATGGTT TGGGAGGCCA CAGGGCATTG TGGCTTTGGG CGGGGCTTTC AGAAGCATGG 600
TGACTCAGCT CTGGGGAAGT GGCTAAAATA GGCTGCCCAA CGTGGGGCAG GCACTCCCCA 660
TAGCCTGCCT TGGGCGGGAC ACCCCCACCC CACCCCAGAA ACCACATCCC ACTTTCTTGG 720
CAGGGAGAGG GAAAATGGAT CACAGCTCAC AGCCCTCCCT AGCTCTCCTG AGCCTCCGGA 780
GGAACAGATT CCTCTACCCT CAGCCCACTG ACCACGGAAC CTTCCTTTAA GGTGGGAACG 840
AGGAGCCCTC CCCAGAAGGT CAGGCCCCTG CTTGGGTCAC AGCAACCACA CCTTTAGTTC 900
AGCCCTGTTC CTGAGACTAC GGAAGACCAC CCTTGCCTGG ACCCCTCGCC TATCCTCCCT 960
GGCCCTCCCA GCTTGGCCAG CCCAGCAGAC CCAGAGCAGA AGGACAGACG GGACCAACAC 1020
TTCTCACTCC AAGTGACCGG GCAGTGGCCT GTCCCTGGCA GCTTGGCTTG AGGCAGGCGC 1080
CAGACCTGAG CTCTCATGGG GCAGCTAGGC AGGCCTCGCT CTCTGAAGCT GCCCTGCGGT 1140
TCACCCCGGT ATACAGGGTA CACAACATGC CTCAATGCCC ACTGCCACTG CCTCCGCCAC 1200
TGCTGCTGGG CAGCATGCCC TCTGCAGGGC CTTCCCCTAG CTGTTCTAAC CAACCACCCG 1260
ATGCCAGGTC CAGGCAATGT GGCCGAATAG CAGAGGGCTT TTAGTGCACG ATGACTTTAG 1320
TTGTGACCTG GATCGGCTAC AAGAGGCTTT GTTCCATTAC TCATCATCCA GTCACTCACT 1380
CCATGACTTC CTGCAGACCC ACTGATATTC ACAAACTCTT CTAGGCCCTG GAGATAGAGC 1440
AGTGAAAATA GCACGCTGTT TTCCCAGGGC ACGTGTGTAG TGTGAGTGTG GGGGGTGGGG 1500
GTGGGGAATG GAGGTGTAAA CCTATAAATA AAATAAATGG TATCTCATAT TCCTCAGTAT 1560
AAGGAGGGAA AGGGGTGGTA TGAGTGGGTG TGGGAGTCAG GGGGTCTGGG GGAGGCCCCT 1620
CTTGAGGAAG GAGCATCATG AGTTGAGAAC CAAATGATGA GAAGGAACCA GCCGGGTCAG 1680
AAGCGACCCA GGCAGAGGGA ACGGCGCGTG CAAACGCCGG GGTATAGGAA CAGGCTTGTG 1740
GCATTTATGG AATAGAATAA AAATCCATGC AGCCAGGGCC CAGGTTACAT AGAGCCCTCC 1800
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