| Tag | Content |
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EnhancerAtlas ID | HS158-00741 | Organism | Homo sapiens | Tissue/cell | Pancreas | Coordinate | chr1:17907860-17908900 | | | Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
| SE_01537 | chr1:17907755-17910530 | Aorta | | SE_23081 | chr1:17907816-17910457 | Colon_Crypt_1 | | SE_23747 | chr1:17907830-17908823 | Colon_Crypt_2 | | SE_24767 | chr1:17907837-17909560 | Colon_Crypt_3 | | SE_26139 | chr1:17906023-17909400 | Duodenum_Smooth_Muscle | | SE_26573 | chr1:17907965-17909539 | Esophagus | | SE_28131 | chr1:17905874-17909536 | Fetal_Intestine | | SE_29073 | chr1:17905814-17909766 | Fetal_Intestine_Large | | SE_31687 | chr1:17907755-17908906 | Gastric | | SE_34117 | chr1:17906048-17909807 | HCC1954 | | SE_47562 | chr1:17907792-17908882 | Pancreas | | SE_50079 | chr1:17907831-17909680 | Sigmoid_Colon | | SE_52601 | chr1:17907734-17908893 | Small_Intestine | | SE_65277 | chr1:17905681-17911473 | Pancreatic_islets | | SE_68684 | chr1:17907877-17909598 | H9 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AACAAAATTA TTCGTCGTTT ATCTGAAATT CAAGTCTGTG TCCTGTATGT TATTTGGCAA 60
CCCTGGCACT GGGGCCTCAG ACACTGCAGG TGGAATCCAG GCCCCGCCTG GGAGGAAATG 120
GGCCCAGGGC TGTTTCACCC AGGCAGCAGC TTCCTGTCCT CTTGTATCAC TATGAGAGAG 180
GCAGAATTGC AGATGGTAAT GAGTGAGGGC TTTGTCCTCA GCCCCATCTG AGTTTGAATC 240
CTGACCCTGC CACTTAGACT GTGGGGCTGG TTAAGTGACA TGTTGTCTCT GTGGCTTAGT 300
TTCATCATCA GTAAACATGG GGACAATGAT ACCCTCTCCT GGGCTGTTGC AAGGTTTAAA 360
TATATGTCAG GCGTGGGCAT GGGGTAATCA ATTGCTCACT GACGGGAGTG CTTATCATCG 420
TGGGTGTCAG CAGGACAGAC AGCGTGTGCC ATGCCCTGCA CCCCTGGGAG AGCCAAATGA 480
TGCATCTCCT CCTCCCTGAG CCTCGGGGTT CTTCTTGGGC GGGGGGTGGG GAGCAGCACA 540
GCAGACCTGT CTTCCCTGTG GCAATGGGTG GCTTCCTAGG GTCCCTCGCC TCCTGGACTC 600
GCTTGTATTT TCTCACAAGG ACCGGGTCTG TCCAGGAACA TCAGAGGCAT GAGTGACCAG 660
CTCTGGCTGT GCCACCTTTG CAGGCTATTA GGAAGGGCTT CCTTCAGCTC TCAGCTGTGC 720
TGGGATGGGC CTCCTGAGTT TTCCTTCTGA TAAGGAGCAA TGCCTGATTG CCGGGGGGAG 780
GATAGAAGGC GGCCTTGGAG ACAAGCACAT CTCACCTCCC AATTCATGAC TGGGATTTGG 840
GTCCCAGCAT GCCTGGCCTT GCCCCATCCC GCCCCTGCTG CCATGGGCAC CTGTTCCCTT 900
TCCTCTCCCC ACCAAGAGGC CTGAACCTGA ACATGGGGAG TGAGAAAAAA AAATTTATGA 960
CTAAGTCAAT TCTGTTCTGT TCAGCAAACA TTTGACAAAT ATTTGTTGTT CCAGCTCTTT 1020
CTAATATTGC TGGCTAGTAT 1040
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