| Tag | Content |
|---|
EnhancerAtlas ID | HS047-22571 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr22:29213650-29216260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr22:29213773-29213791 | CTTTCCTGCCTTCACTCC | - | 6.38 | | Nkx3-2 | MA0122.3 | chr22:29214817-29214830 | ATTAAGTGGATTT | - | 6.2 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_13369 | chr22:29213933-29215319 | CD34_Primary_RO01536 | | SE_14087 | chr22:29214035-29215210 | CD34_Primary_RO01549 | | SE_14873 | chr22:29214026-29215269 | CD4_Memory_Primary_7pool | | SE_23503 | chr22:29213954-29216233 | Colon_Crypt_1 | | SE_25378 | chr22:29203596-29221521 | DND41 | | SE_26202 | chr22:29213735-29216427 | Duodenum_Smooth_Muscle | | SE_28436 | chr22:29213969-29216417 | Fetal_Intestine | | SE_29251 | chr22:29213623-29216355 | Fetal_Intestine_Large | | SE_31018 | chr22:29212584-29216265 | Fetal_Thymus | | SE_31638 | chr22:29213521-29220117 | Gastric | | SE_33938 | chr22:29213595-29216692 | HCC1954 | | SE_35317 | chr22:29213576-29216650 | HepG2 | | SE_43412 | chr22:29213616-29213939 | MCF-7 | | SE_43412 | chr22:29214010-29216682 | MCF-7 | | SE_43527 | chr22:29212224-29222080 | MM1S | | SE_47780 | chr22:29213966-29214887 | Pancreas | | SE_47780 | chr22:29214959-29215289 | Pancreas | | SE_47780 | chr22:29215309-29216217 | Pancreas | | SE_50644 | chr22:29214010-29216455 | Sigmoid_Colon | | SE_52811 | chr22:29213951-29216307 | Small_Intestine | | SE_54242 | chr22:29213988-29216044 | Spleen | | SE_55644 | chr22:29214183-29214876 | Thymus | | SE_55644 | chr22:29214944-29215620 | Thymus | | SE_62966 | chr22:29186510-29220159 | Tonsil | | SE_67157 | chr22:29212224-29222080 | MM1S |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 29215320 | 29215875 | | chr22 | 29214079 | 29215240 | | chr22 | 29215471 | 29215733 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I028807 | chr22 | 29203221 | 29221297 |
|
Enhancer Sequence | TGATCTCAGG TGATCCACCC GCCTCAGCCT CCCAAAGTGC TGGGATTACA GGCATGAGCC 60
ACCATGCCTG GCTGATCCTG CTAGATTTCT GTCTCTACTT ATTTTAACTC TTGTCCTTTG 120
TCTCTTTCCT GCCTTCACTC CAGCCCCTTC AAGACTCCCT TAATATTTCT CTTTTAACCA 180
ACTTTTTTTT TTTTTGAGAT GGAGTCTCGC TCTGTTGCCC AGGCTGTAGT GCAGTGGTGT 240
GATCTCAGCT CACTGCAACC TCCGCCTCCC AGGCTCAAGC GATTCTTGTG CCTCAGCCTC 300
CCGAGTAGCT GGGATTACAG GCGCCCACCA CCACGCCCGC CTAATTTTTG TACTTTTAGT 360
AGAGACGGGG TTTCACCGTG TTGGCAACTC TGGTCTCGAA CTCCTGACCT CAGGTGATCT 420
GCCTGCCTTG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGTCACCTCA CCTGACCTTA 480
ATAAACAACT TGTTTTAAAA ATGGGAGGCA GGATGTGTGT ATGTGTGTGT GTGTGTGTGT 540
GTGAGAGAGA GAGAGAAAGA GAGAGAGAGA GAGAAAGAAT ATCCTTCCCC CACCTCTGCA 600
ATTGGCCTTA AATTTTACAC ACTCACCACC CCTACTTCCC TGCTTTGATG CTGTCCCTAA 660
AGCAGTGGGA AAGAGCTTCA GGTCTCTGAG CTTGACCAGT GTTTCAGCTC TCCCTTGGAG 720
TCCCGGGAAA CGTATCTCTT GGGATCAGGA GCTGGGATGG AACCCAGGGC TCCTGAGATG 780
GGACAAAGCT ATGCTCTGTG CACCTGTCTT GCCTCCTCAC TTTGTACAAT GAGGTAGGCA 840
ACCTTTTGTA TTTCCTCTTG TTTTCTTTCC TCACCCCACT TGGCGTGGCA GCCATAAATC 900
CAGTTTCCTC CTTGGCATTT CTTAAATGTG TTCTGCCTGA ATTAAAAACT GAAAGGGGGG 960
AGGCCCAGTA GACCTTGAAA TGTTCAGCTT GCTTTCTGTC CTTGGCCACT GGCTTGACAG 1020
GTCCCACAAG CTCTCCTGGG AGAGTGAGCA GCTGACGAAA TCCCAGAGGC CCTGAAACCT 1080
CCCTTCCAGT AAGTGCCCAT GTTTGCATAT CCTGGTTCAA GAATAGGAAC TGCTTGATGG 1140
AAACTGATCA GGGAGCTAAA ATTACTGATT AAGTGGATTT GCTTCCAGCT GCAGGCAGTG 1200
GCCTTCCTGA GAAAGAGGGA ATCTGTAGGG CTGTTTTTAC AGATTAAGAT CTGCCTTGTT 1260
TGTTCACTTT CTATTTCTAA AAGTTCTTGG AACCCTTTTC TAGGAAGAAG CCAGGTAAAG 1320
TCAGAGTAGG GAAAAACAGT AAGCCTTGTT TTTGTCCTCT ATACTTTAAA GCTTCCTTTA 1380
TTTTCAAAGA GACATACATG AGATATCTGA AATAAGTCAG CTTTAGGAAG GATAGCTAAC 1440
GAATGTTGGA TGTATGCTAG GCACTGTGTG AGCACTTGGC ATCCATTCTC TCTTTGGTTC 1500
CCGCAAGTTA GGAATTGGCC CCTTTTCTCA GAGGAGAATG AGGCCCTGTG AGGTTAAGCT 1560
GATGACCATG AAATTGTCAG TGGTGGAACT GGGATCTTAT TATTATTATT ATTTTGAGAC 1620
AAGGTCTCAC TCTGTCGCCC AGGCTGGAGT GCAGTGGTGT GATCACAGCT CACTGCAGCC 1680
TCTACTTCCC AGGCTCACGT GATCTTCCCA CCTCAGCCTC CCAGGCAGCT GGGACTACAG 1740
GTGTAAACCA CCATGCCCTG CTAATGGAAC TGGGATTCAA ATCTAGATTC CTTGCCCCGT 1800
GTCCTGGAGG TTGCCCAGGC ATGGAAAAGA TCCAGGCCTG GTCCACTGCT TTTAGACACT 1860
TCTCAGGCAA CCCCCTCTTT CAGTAATTTG CGTTTGATTA GATAGAAACT GAAAACTCAT 1920
GTCAAGGTGT CTGAAACCAG CAAAAGAATG TTTTTTCATC TTTGTCCCCA TTCCTTGGTT 1980
GGAGGGGGTG CTGGGTGACA TTTGCTGTGC AAACAATAGC CCAGAAGCCG GGCAGAGTCC 2040
ACACCTAGCT GAGTAAATAG CACCTGAAGG CCCTGGCAGG GCATGCAAGC TCCCCAGGGG 2100
TGCCTTGCTT TGAGAGACAA CCATGAGAAT GTGCCCTTGG ACTGGAAGCC AGGAATCCAG 2160
AGCTGTAGTC CTAGTTCTAC TGTTATTAAC ACTTGCACCT CTCTGTTCCT CATCTTTGAA 2220
GTGAAGAAAA CCAAGTTGAT GATGTTTGAG GCCTGAGGCT GCAGGGGTCA GTTTGACTTA 2280
GGCAGTGCAG CCTGGTGGTT AGGCACACAC AGAGTAGAAT CCAGTTGCCT GGGGTCCAGT 2340
ATGAGCTTCA TGGCTGGACA AGGTGGCTCA TACCTGTAAT CCCAGCACTT TTGGAGGTCA 2400
AAGTGGAAGA CCAGAGTGGA CAACAGAGCA AAACCTCATT TCTACAAAAA ATAAATAATT 2460
AGCTGGGCAG GGTGGTGTGC ACTTGTAGTC CCAGCTACTT GGGAGGCTGA AGTGGGATGG 2520
GAGGATTACT TGAGCCCAGG AGTTCAAGAC TACAGTGAGC TATGATCACA CCACTGCACT 2580
CCAGCCTGAG TGACAGAGCA AGGTCCCGTC 2610
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