Tag | Content |
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EnhancerAtlas ID | HS061-00391 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr1:23903810-23905260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr1:23905153-23905164 | GTTTTATTGGT | - | 6.32 | Nkx3-2 | MA0122.3 | chr1:23905146-23905159 | ATTAAGTGTTTTA | - | 6.16 |
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| Number of super-enhancer constituents: 40 | ID | Coordinate | Tissue/cell |
SE_01721 | chr1:23900657-23905229 | Aorta | SE_02313 | chr1:23901876-23905526 | Astrocytes | SE_03649 | chr1:23903960-23904459 | Brain_Angular_Gyrus | SE_04396 | chr1:23902891-23904726 | Brain_Anterior_Caudate | SE_05716 | chr1:23903816-23905335 | Brain_Cingulate_Gyrus | SE_06239 | chr1:23900696-23905116 | Brain_Hippocampus_Middle | SE_07293 | chr1:23902637-23904795 | Brain_Hippocampus_Middle_150 | SE_08579 | chr1:23902794-23905344 | Brain_Inferior_Temporal_Lobe | SE_10300 | chr1:23899372-23906111 | CD19_Primary | SE_11050 | chr1:23898822-23908436 | CD20 | SE_18996 | chr1:23902922-23905455 | CD4p_CD25-_Il17-_PMAstim_Th | SE_26335 | chr1:23902515-23905797 | Duodenum_Smooth_Muscle | SE_27258 | chr1:23902880-23904675 | Esophagus | SE_27884 | chr1:23903017-23904621 | Fetal_Intestine | SE_28880 | chr1:23903194-23904813 | Fetal_Intestine_Large | SE_29676 | chr1:23901788-23905238 | Fetal_Muscle | SE_31953 | chr1:23903835-23904596 | Gastric | SE_34689 | chr1:23902272-23905407 | HeLa | SE_37153 | chr1:23901250-23906299 | HSMMtube | SE_38016 | chr1:23903113-23904896 | HUVEC | SE_38999 | chr1:23901867-23905446 | IMR90 | SE_41075 | chr1:23901556-23905295 | Left_Ventricle | SE_42328 | chr1:23901634-23904721 | Lung | SE_42328 | chr1:23904726-23905233 | Lung | SE_44435 | chr1:23902863-23905477 | NHDF-Ad | SE_45797 | chr1:23901058-23906146 | Osteoblasts | SE_48755 | chr1:23902917-23904674 | Right_Atrium | SE_50077 | chr1:23902728-23906171 | Sigmoid_Colon | SE_51741 | chr1:23901781-23905632 | Skeletal_Muscle_Myoblast | SE_52549 | chr1:23902842-23905170 | Small_Intestine | SE_53706 | chr1:23902697-23905306 | Spleen | SE_54840 | chr1:23900793-23905744 | Stomach_Smooth_Muscle | SE_55341 | chr1:23903829-23904379 | Thymus | SE_56054 | chr1:23901526-23905401 | u87 | SE_58372 | chr1:23873313-23964782 | Ly1 | SE_63528 | chr1:23901642-23905713 | HSMM | SE_68324 | chr1:23879596-23905390 | TC32 | SE_68325 | chr1:23879596-23905390 | TC32 | SE_68477 | chr1:23874949-23904689 | TC71 | SE_68478 | chr1:23874949-23904689 | TC71 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I023572 | chr1 | 23899427 | 23906089 |
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Enhancer Sequence | AAAATTCTTC CAGCTTAAAA AAAAAAAAAA AAAGCTATTA AAAGAAAGTA AAAGTTTCAA 60 AACCAAATCC TAGGCAAACA ACCCTGAAAA CAATACACAC ACATACATAT ACATACAGCA 120 CCCAAGGTAG CTCTGAGAAC AGGATATGAA ACCTTGCAGG CCGGCACTAA GAAATGATTC 180 ACAGGCCTTT GAGATGCTTC TATTTCAAGA CACAGTCCAC CCACTGGATC TGGTGGCTCC 240 AAAAACAAAC TTTCAGCTGC TGTTTCTTAT CGCAGTGTGG TTCGCCTGGC CAGTATCCTT 300 GGGTCTCAAG AGCTCCAGAC AGAAGACAAG GTTGAGTCCT GTGAATTCCC TTTCTGTTCT 360 ATTTCAAGCC TCAAGCTGCT GGCTTGTTTA AAGAAAGTCT TTTGCATCCA CCTTTTGGTT 420 GGCTGACCCG AGTTTAAAGC AACATAGCCT AATGGGTTCG TAGCACAGCC TGCGAATTCA 480 TAATTTTAGT TTAGCAAGGC CTCTGTGTGG CTCCAGCAAG TCCTACTGGA TCCTGGGCTG 540 GTCATTCTAG AAGCTGTCTC CAGCTAAACA ATCCTGCCTG GCTTTCCTTA TACATATCAA 600 TATTATACTT GCCCTAGGCC AGGATTAAGA ATTTTAGCAC AAATTCAAAA TTTCATGCTT 660 TTATGTAAAA TAGAAATATA AAAGTAATTC ATTCGATGAA ATGCTTACTG AGTGCTCACT 720 ATATGCCAAG CACCAGCAAT GTACTGGCGA TAAAATACAG CCCCTGCCTT CAGGAGCCAC 780 ATTGAACAGG AAAAGCAGAC AATCTAAATA TACATAGTAG AAACACATGG AACTATTCCC 840 TATGGGAAAT GCCCTGCATA AAAAGTGATA CCAAAGTTGG AGCAAAATTG AAAGAAATGC 900 AAATGCTTGT GATACGGTTA AGTACATTTT CATCTGTACT TACCCTTGAT TTTGTTTTAG 960 ATTTAGAAAA TCTTGAACTT TCACTGTTGC TTCATTTGCC CTCCAAAAAT CCAGAATCTT 1020 ACAGAAAGGG TCAGTGTCTG GATCAAACAT GTTTCTTATC TAATTTCCTT GCCCCAGTTT 1080 TTGTTTATGC CATCATTGCT GCATGGAGTC CTCCCTCCTC TCCTTGTGTA TCCTCCAAGT 1140 TCTGATGCAA AGCCCACTTC CTCCAGGAAG CATTCGCAGA CCCATCTGGC CACATCCTCG 1200 CTGTTCTCTA AACACACATA TCTCATGCTC TTGACTTGGC CTTTAGCCTG TCCTGCCTTA 1260 TGATCTCTCT TGTACTTCTG TCCTGAAGTT TTATCTAACT TATGAATTGG GGGAAAGAGG 1320 ACAGGCACTG ACATTTATTA AGTGTTTTAT TGGTGACGGG CATTTTGCTA GCTCTTTACT 1380 GTATATAATG TGCCTGGTAT GTAGAAGATG TTCAATAAAT ATTTGTTCAA CGAATGCTTC 1440 AGTGATTTGG 1450
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