| Tag | Content |
|---|
EnhancerAtlas ID | HS051-00219 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr1:12508830-12511850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR3C1 | MA0113.3 | chr1:12511524-12511541 | AAGGACATTTTGTTCCT | - | 6.08 | | NR3C2 | MA0727.1 | chr1:12511524-12511541 | AAGGACATTTTGTTCCT | - | 6.27 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_00009 | chr1:12506389-12526105 | Adipose_Nuclei | | SE_01743 | chr1:12508791-12509347 | Aorta | | SE_01743 | chr1:12509733-12511495 | Aorta | | SE_01743 | chr1:12511532-12515011 | Aorta | | SE_03005 | chr1:12508948-12509464 | Bladder | | SE_03005 | chr1:12509717-12510109 | Bladder | | SE_15065 | chr1:12506299-12515319 | CD4_Memory_Primary_7pool | | SE_20910 | chr1:12506384-12515111 | CD8_Memory_7pool | | SE_26086 | chr1:12506439-12510424 | Duodenum_Smooth_Muscle | | SE_26716 | chr1:12506659-12513255 | Esophagus | | SE_28215 | chr1:12507888-12510030 | Fetal_Intestine | | SE_29231 | chr1:12507637-12510111 | Fetal_Intestine_Large | | SE_29871 | chr1:12507739-12511538 | Fetal_Muscle | | SE_33776 | chr1:12506505-12516452 | HCC1954 | | SE_37319 | chr1:12506164-12510707 | HSMMtube | | SE_39244 | chr1:12508337-12510202 | IMR90 | | SE_39882 | chr1:12506572-12512625 | K562 | | SE_41209 | chr1:12508082-12512128 | Left_Ventricle | | SE_42647 | chr1:12507839-12509412 | Lung | | SE_42647 | chr1:12509663-12511484 | Lung | | SE_42647 | chr1:12511538-12515195 | Lung | | SE_45864 | chr1:12506318-12510756 | Osteoblasts | | SE_49026 | chr1:12508155-12509308 | Right_Atrium | | SE_49026 | chr1:12510064-12511360 | Right_Atrium | | SE_50544 | chr1:12507931-12511360 | Sigmoid_Colon | | SE_51539 | chr1:12506369-12511986 | Skeletal_Muscle | | SE_52815 | chr1:12507938-12510555 | Small_Intestine | | SE_54847 | chr1:12507468-12511742 | Stomach_Smooth_Muscle |
|
| | 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 |
| GH01I012446 | chr1 | 12506572 | 12511845 |
|
Enhancer Sequence | ATCCTTTTTA AGGAAAAAGC AAAATCCTAT TATGGGAATG CTTCAAACCA CTCTGAGCTT 60
CCAGATTAAT CTGAAACAGC ATCTGAGTTC ACAACTGGGT CAGAGTTGCA GAATAGCAAG 120
AGAAACTTGC CAGTTCAGCA GGCGTGTGTC TTGGGTTAGT TAAGACAGCA GGACAGTCCT 180
GAGGCCTGAC TTCCTTGCAT GTGTTTCAAC CTTGGGTGCT GAGATAATTC TGGGTGGCTT 240
TAGATAACTT TGTTTCTTAA CTGAAAAAGG AGTGTCTGTT GCCTGATAAG TGTTTATCCG 300
TGAAATAGCA ACATGGTGTG CATCTTAGGG TAGGAGGGCT TTTAGATCTC CAGAGACCAG 360
GAAAAAAAAA AAAGCAAGGT CATTGGCTTA GGCATATTAC TGGAATTAGG ATGTCAGTCC 420
CAACTTTAAA ATGCCTGTAT TGTTTTTATT CAGGGTCCCC TTTCTGGATT CCTCCCCTTT 480
TTTTCTCTTT GCCTTAAGGG CTATACATAA TCCATAACCA AGTAGAACTG AAAACAGACA 540
AAAGCACTCC TCTTCTAGTG GATAGAAATC TGGAATCCAG AAATGCTTCC TTCTTGCCAA 600
ACCTCAACTT GTTCCGTGCC TTTTTTTTTT TTTTAAATGC CTCTTCCCAG CCTCCCCACC 660
CTTTCGTGAT TTGGCTGAGT GAGGACTAGC TGTTTGGTTT GCCTTTTATC AACAATAGAT 720
ATTCACTGCT TTTCAGGTCA CATTTTCCTT TAACTCTTCT CTGTTTATGA GTATCACAAA 780
AGGGTTCTTC AACATCAAGG CAAAACTCAC ACTCAGAATA CTTTTTAACT GTGGATATTT 840
TGACAGTATG AAACGGAAGT CAGTGGTGAA GACTTTCGTT TTGAAGTGAC TTAGGTCTTA 900
CATGACTCAA AGATGGTTTT CCTAGTAGTA TACCAGCAGA GTTGAAAATG ACTCTGAAAT 960
TGAAAGTCCC ATACTACTTC TAAGAAACTT GTAAAAAGTG TTGGCCAAAT GCTACACCAA 1020
ACATTTTGCA TTAATTATTC TCTTAACTCT TCAAAACAGT CCTTTGCAGG CCAGGCTCGG 1080
TGGCTTATGC CTGTAATCCT AGCACCTCGT GGGGCCGAGG TAGGCAGATC ACATGAAGCC 1140
AGGAGTTCAA GACCAACCTG GCCAACACGG TGAGACCCTG TCTCTACTAA AAATACAAAA 1200
ATTAGCCAGG CGTGGTGGCA CACAACTGTA ATCCCTGCTA CGGGAGGCTG AGGCATGAGA 1260
ACCGCTTGAA CCCAGGAGGT GGAGGTTGCA GTGAGCTGTG ATCGCACCAC TGCACTCCAG 1320
CCTGGGTAAC AGACTGAGAC TCAGCCAGCA AAAAAAAAGA GCAATCCCTT ACAGTAGAAA 1380
GTATGTGATT TTAGCAGATG GATAAACTGA GGTTCAGAGA AATTAAGCCT CTTCCACCAG 1440
CATGCGTGTT TGGTAACTGT CAGGGTAAGA TTTGATTCCT TTGCTCCTGC TTGTTTGACT 1500
ACATCGTGGC AACTCCCACA AAGTTCATGG CAGCCTTACT TAGAGGCACA ATAGATAGTT 1560
GGGTTTTCCA AATTTATGAG TTCAGACATA GCTTATTGCA GGCAATGCTG ATTAGAATTA 1620
GAGCTGTGCT GGTAGCTGAG GTTTGCAGCT GTACAACCTT GTATAGTCTC TGACTTGTGG 1680
TGGTTTAACT TACAATTTTT TGACTTGACG ATGACGTAAA AGCTATATGC ATTCAGTAGA 1740
AACTGTACTT CAGATTTTGA GTTTTGATCT TCCTGGGCTG GTGACATGTG ATCCGATTCT 1800
GTCGCAGTGC TGGGCACTAG GGCAGCCGCA GCTCCTAGTT AGCCACGTGA TCATGAAGAG 1860
GGAACAAATA CTCTACAGTG GGCCCTGCTG CCAGATGACT TCGCCCAGCT GTCAGCTAAT 1920
GTAAGTGTTC CGGGCATGTT TAGATATGTT AGGTGTATGA AATTCATTTT TACTTAAAGC 1980
CTTTTCAACT TAAAAATGGG CTTACCCGGA CGTAATCCCA TCATAAGTCA AGGAGCATCT 2040
GTACTTGGAA GAATATAAAA CTTCTCCATC ACACTACGGA GTCCTGCCAC TTCTCTCTTT 2100
TCCTGTTGTA TTTGGTTACC ATCTTCCCTG GTGACAAGGA AGATACTGCC ACCAGCAATT 2160
ACTCAGTGAG GCAAAGATAT TAAAGAGGAA ATTTCCATTA GGTAAATAAC TGTGAAAGAA 2220
GAACCCAAGA GAAGGGAGAG AAATTCAAGC CCCAGCTCCT GTTACACTGG CCAAATGCCT 2280
TTGGCACCCC ATGCTTGCTG AAGATCATAA AAGGGTCAGG TAAACTGATC AGACAGAACA 2340
GAGGAACACA GTGTGAATTT TTTCCCTTGC CCCATTCCAG TGTCTACTTG AATTTCAGTT 2400
TTAGAAAATC AACCCTTCGG AGCCAGGCCC CAAACCCAGG CTAATTTGCA GTGTCTCCAT 2460
TTGTGTAGAC AATGAGATTA TTTTGGGAAG GAGGGTGTTG ACAGAGTGTG TGTTAGCTAT 2520
TCAGTAGAAC TGGCATCTTG AAGTACTTCT GAGATTTTTA CCCCCTTGCT GAAAATATTG 2580
CTTTATAGAA GTTAATGACT TTGGACTGTG GCCAGAATTC ACAAGTATGG CATGTGTTGA 2640
AGTGAAAGGA AGGGGAAAAT CATTGTCTTT GTGAGTGTAA CACTAGATTT TCTGAAGGAC 2700
ATTTTGTTCC TTGGAACCTT TCATTTTAGC TAGAACAACA TGCACTTGAA GCCTTAAGTA 2760
TTTTGTGGAC TTGAGATTGC TACAAAATGA GGTAGGCAGA CTTAAGTCTC TGCAAATGCT 2820
CCTTCTGGTG TTAAGGTATT ATAACCAAAG AGTTACAAAT TGTCTGCAGA TTACCTTCCA 2880
GTTGCTAGTC GCTTTCCCAG TTTAGAAGCC TAGCACACCC TGGTGCTGTT ATGCCCTGCT 2940
GCAGATAGCT TCCGCTTTGC TGGGGGGATA TGCCATGCCA GATGCTTTAC GTGCACACTA 3000
TCCCTGAATC CTCAAGACAG 3020
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