| Tag | Content |
|---|
EnhancerAtlas ID | HS184-13120 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:17600200-17603390 |
| | Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
| SE_00905 | chr17:17599859-17602812 | Adrenal_Gland | | SE_00905 | chr17:17602813-17604413 | Adrenal_Gland | | SE_02229 | chr17:17599636-17601520 | Aorta | | SE_02900 | chr17:17600931-17602833 | Bladder | | SE_03155 | chr17:17600160-17601136 | Brain_Angular_Gyrus | | SE_23508 | chr17:17599848-17601610 | Colon_Crypt_1 | | SE_23959 | chr17:17600190-17600829 | Colon_Crypt_2 | | SE_24961 | chr17:17600095-17600929 | Colon_Crypt_3 | | SE_26187 | chr17:17596287-17601342 | Duodenum_Smooth_Muscle | | SE_26187 | chr17:17601645-17603824 | Duodenum_Smooth_Muscle | | SE_26567 | chr17:17599593-17604166 | Esophagus | | SE_31385 | chr17:17599815-17602843 | Gastric | | SE_31385 | chr17:17602945-17604168 | Gastric | | SE_33924 | chr17:17599806-17601771 | HCC1954 | | SE_34327 | chr17:17599901-17600609 | HCT-116 | | SE_34327 | chr17:17601681-17602494 | HCT-116 | | SE_36431 | chr17:17599801-17601354 | HMEC | | SE_42078 | chr17:17599658-17603752 | LNCaP | | SE_42180 | chr17:17594201-17604768 | Lung | | SE_43483 | chr17:17598056-17600741 | MCF-7 | | SE_43483 | chr17:17600770-17602893 | MCF-7 | | SE_46499 | chr17:17601745-17603723 | Osteoblasts | | SE_47257 | chr17:17592191-17603274 | Panc1 | | SE_47490 | chr17:17599863-17600648 | Pancreas | | SE_47490 | chr17:17601123-17601706 | Pancreas | | SE_47490 | chr17:17601716-17602190 | Pancreas | | SE_48869 | chr17:17599644-17603937 | Right_Atrium | | SE_49608 | chr17:17599806-17600787 | Right_Ventricle | | SE_50171 | chr17:17599701-17601723 | Sigmoid_Colon | | SE_53329 | chr17:17599594-17602895 | Spleen | | SE_54742 | chr17:17595926-17603895 | Stomach_Smooth_Muscle | | SE_63253 | chr17:17584631-17604117 | GLC16 | | SE_65592 | chr17:17593958-17606061 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 17601421 | 17602689 | | chr17 | 17600259 | 17600576 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I017689 | chr17 | 17592642 | 17604766 |
|
Enhancer Sequence | AGGCCCCTTG TCGATCCTGT GACCCACCTT CTGCTTTGAC TTCCTAGGAG TTGGTTTCTG 60
CTGCCCTTGG CTCCTCAGCC CCTCTTCTCT AGCCTCTCTC TGGAGGCATG CAGGCTTGGC 120
ACCAGCACAG CCTCCCTCTG CCCAGCTGCC CCTTGGCCCT AGCTACAAGC TGCCCTTGCC 180
CTGACCTATC CCTACTGCCA GGCCTGTCTC TTCTCCCCTA TTCCAGAACG GTTCAATTCT 240
AACACATCCA AGCCCTGCGT GAAACAGGCC TTGGGAAATC ACAGTTGCCA GGGACGGTTT 300
GGCATTTAAA AGGCATCCAA GGCTTTGGGG AAAAAGCTGA AGAGACAAGA GGATGCAGGG 360
CCCTGTATCA GAACAGCATC TGGATTTACT GGATGGAAAA ATCACAGAAT GCCCCTTTCC 420
TCGGGAATAA CAGTCCTGGC CGAGGGGCAG CGGGTGTGGC ATGGGCACGC CATGCCCTGC 480
CTGGCCACCA CCTGCCATCA CCGCTGTGTA CTCTCAGAAA TGAAAAGATT AGGGAAAAGA 540
TTAGGGAGGG ACATTGTCAG CCTGCAGCCA ACGGCCCGCT CTAACAGGTT TATTCAGTTG 600
TAAAATATTT AAGACCTGTT TCACTTTACC TGTATCCAGG AGGCAGCCAG GCTGGGGCCG 660
AGATTGATGT GCTGAACATG ATTTATTTAT CTGGATTTGC TCTTGTGGTC TGGGTGTTAC 720
CTGGGTGTGG AATTTAACCA AATGACAAGA TGGGTTTGCG TGTGTTCCTG AGCTTGGGGA 780
TTGTGTGTGT GTAAAAAGTG AGTTGGGGTT TGTGTACATG GCAGGGGGTT GCTGTTAGGT 840
GGCTTGTGTG TCTGTTTGTC ACTGGGACCA ACGTGTGGTT GTGTGTGTGT CTGATTTGGG 900
GAAATGAGCT GAGGGTATGG GTGCTTACAC ACCAGGCAGT ATCCACAGCA GGTCACACGT 960
TCTTTGTGTG TTGGGGGCAC CTCTGTGTGT GGCCGAGTAG CTGTTTGTGT GCATGTCCTG 1020
TGGTGTGAGA CCTGGATCTC TCTCACCCAC TTTTCATCAG TGGTGGGGCA TTGCGCACTG 1080
ACTGAGTTGC TGGGGCATCT GCTTTTCCAT CCGGCCCTGG GTGAGCACTG ACAACACCTG 1140
ACTGTCTTCC AGTAGAACTG GGCCTTCCTG CCCTGCAGTC CAGAGACTAG AGGGAGTTCG 1200
GTGGTCAAGG TGGTCCAGGC CCACAGCCAT AGCCCTAATG CAAAGCATGG CTCCTACTCC 1260
AGTGCGCTGC TGTGGGGTGA CCCTGCTCCT CCTCCCTGGA CCTCAGTTTC CTCTTCTGCT 1320
GCAGAGGGCA GGCGCCCAGG TCCCTGTGGC TGCTCTCACA CACGGGCTTC TGGGTGGCTC 1380
ATGGCAGGCT TAGGGCATTG GGCTGGGGTT TGTCTCCTGC CACTCAAGAG TTGAGTCCCA 1440
CCAGTACTCA AGAACAGCAA GGAATGATGG GAAAATCCCT GCTTTGGGGC CCAACTCTGG 1500
ATTCTGGGCG TTGTCTCTGT CCCCCATCTA GGCCCAGCCC TGGCCCAGTA GTCAGGAAAG 1560
CGGCAGACAA CCCTGTAACA GCCCTCGGTC TCCCCCTCCC CCCACACCCC TTTATATTGA 1620
ATGTGTCTGT CACTACTTTC CTAATGAGGC TGCTGAGGGC CCCCCTGGGG CAGATACCTT 1680
TGCAGACCGG AGGTGAGGGG GTGGGCCAGC CTCAGGGTCA GGACAGGAAG GGGAGCTGAG 1740
CCCTTCCCCT GCCTGCACCC CCAGGCCAGC TCAGCTGTGG AGGCATTGAG GCCCCTCTCA 1800
GCCCCTGAGC CAGCTGTGAG TGGGCATGAG AGCTTGGGGA GGTAGGAAAG CTCACCCCAG 1860
GCACTGAGTT TTCTTTGGCG CTGTGACTCT GTAGTAATAA TACTTCCACC TGGTCGATAT 1920
CTATGTTTGG AGGCCTACTG TGTGCCAGGC ACTGAGATCA GCCATGATCT GGATGGACAC 1980
ACAAAATCCC TGCCCTTGAG GGAGGTGTGG CCAAAGGAAG AAAGACATTA ATCAAAGAAT 2040
CAAGTGATCT GAGTCGTGCA TTCATGCATG GGAATGCCGG CTGATCACAA GCCAAGACAG 2100
AGGCCAGGCA GAGCTTCTCT GATGGAGACA GGGAGTCCTG TGCTTAGACT GGGGGCTGAT 2160
CCAGGCACTG GGTAAAGGCT CAGCCGGGAT TGAAGGAATC AGGAGACCCA GATTCTTGCT 2220
GTGTGGCCTC AGGCAACTGC CCACCTTCTC TGGGCTCCTA GAGGCTGGTG GCTTCCTTCT 2280
GGCTCCCGTC ACCTCTGAGT GGAACTCAGG CAGTATATGT CTCCTCTTCA GTGCTTTTTG 2340
CGCTCCCTGC CAGGGCCCTC AAGACATCTG TCGGCAACAT CCTTGACTTT GGAATGCTGG 2400
AGGCACTGCC CCAGGGGACG CCTGGAGCCA AGCACAGCAC CGCTGCCTCA GGCCCCACCT 2460
GCCAGTTCCT CTGGGCCCTT TTGCTCTCAC AGAGCCACCT GGATCGAAGA AAGCCTGGAA 2520
AACATTAAAT TGAAGAATTA GTCCCCTATT TTGCCCCAAA ATTGCAGAGA AAAGCATTTA 2580
TTCATGCATT CACTCATTCA TTTGCTTGAC TAGTGTTTCC TGAACACCTA GTAATTGCTG 2640
GGCACACTGC ACTCCATGTT GGACTGAGAT GGCAAAGTGG TGGTCCTCCT GCCACGTCCT 2700
GACCACAGAC CTGTTTTGAA AGCCCATCCA TTGTCGGGGG GCCGGGGGGG GGGGAATCAA 2760
ATGAATTGCC AGTGAGTAAT CGTTGAGTGA CTTCATTTCC AATTTCCAGT TTACATTTCT 2820
TCTGGATTAT TCTACCCTGC TTCCCCCGGC CACAGTTGGT GGAGATGGCT ACTGTCTGCC 2880
GGGTAGGATG GCCCACCCAG CCCACCAGCT GGTCACGGTC CCATCCCCCA CCACTCCACC 2940
CCACCCTGTG CCTCTCCTGG TCATGTCACA CATGATAGTG TGGCTTCCTA GTTATGAGCC 3000
CAGCCTCAGG AGCCAGACTG TCGAGGTTCA AAGCTCACTG TGGCTTGTGG GACCTTGGGT 3060
GTCCCCCTCC AAGCCTCAGA TTCCTCTTGT GTAAAATGGG ATCACAAGAG CAAGTATCCA 3120
CTACTCCTGG GGCTCTTGGG GAGATTAAGT GAGAAAATTT ATGCTAAATC CTTAAAACTC 3180
ACATAAGCCT 3190
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