| Tag | Content |
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EnhancerAtlas ID | HS182-00324 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr1:17907870-17908980 | | | 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 | TTCGTCGTTT ATCTGAAATT CAAGTCTGTG TCCTGTATGT TATTTGGCAA CCCTGGCACT 60
GGGGCCTCAG ACACTGCAGG TGGAATCCAG GCCCCGCCTG GGAGGAAATG GGCCCAGGGC 120
TGTTTCACCC AGGCAGCAGC TTCCTGTCCT CTTGTATCAC TATGAGAGAG GCAGAATTGC 180
AGATGGTAAT GAGTGAGGGC TTTGTCCTCA GCCCCATCTG AGTTTGAATC CTGACCCTGC 240
CACTTAGACT GTGGGGCTGG TTAAGTGACA TGTTGTCTCT GTGGCTTAGT TTCATCATCA 300
GTAAACATGG GGACAATGAT ACCCTCTCCT GGGCTGTTGC AAGGTTTAAA TATATGTCAG 360
GCGTGGGCAT GGGGTAATCA ATTGCTCACT GACGGGAGTG CTTATCATCG TGGGTGTCAG 420
CAGGACAGAC AGCGTGTGCC ATGCCCTGCA CCCCTGGGAG AGCCAAATGA TGCATCTCCT 480
CCTCCCTGAG CCTCGGGGTT CTTCTTGGGC GGGGGGTGGG GAGCAGCACA GCAGACCTGT 540
CTTCCCTGTG GCAATGGGTG GCTTCCTAGG GTCCCTCGCC TCCTGGACTC GCTTGTATTT 600
TCTCACAAGG ACCGGGTCTG TCCAGGAACA TCAGAGGCAT GAGTGACCAG CTCTGGCTGT 660
GCCACCTTTG CAGGCTATTA GGAAGGGCTT CCTTCAGCTC TCAGCTGTGC TGGGATGGGC 720
CTCCTGAGTT TTCCTTCTGA TAAGGAGCAA TGCCTGATTG CCGGGGGGAG GATAGAAGGC 780
GGCCTTGGAG ACAAGCACAT CTCACCTCCC AATTCATGAC TGGGATTTGG GTCCCAGCAT 840
GCCTGGCCTT GCCCCATCCC GCCCCTGCTG CCATGGGCAC CTGTTCCCTT TCCTCTCCCC 900
ACCAAGAGGC CTGAACCTGA ACATGGGGAG TGAGAAAAAA AAATTTATGA CTAAGTCAAT 960
TCTGTTCTGT TCAGCAAACA TTTGACAAAT ATTTGTTGTT CCAGCTCTTT CTAATATTGC 1020
TGGCTAGTAT CATCTGGGTG AACCCAGCTC TTTGCCATTT TCTCATTCTC TGAGAGCTTC 1080
CCATTACCTT CCCAAATTAA ATTCAAATTC 1110
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