| Tag | Content |
|---|
EnhancerAtlas ID | HS045-03853 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:154399770-154401570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr1:154400148-154400162 | CCCCTTTGATGTCT | - | 6.14 | | ZNF263 | MA0528.1 | chr1:154401281-154401302 | TGAGGAGGAGAGCGAGGGGAG | + | 6.42 |
|
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_00437 | chr1:154399481-154401751 | Adipose_Nuclei | | SE_01040 | chr1:154399528-154400582 | Adrenal_Gland | | SE_01040 | chr1:154400681-154401626 | Adrenal_Gland | | SE_06653 | chr1:154399347-154403450 | Brain_Hippocampus_Middle | | SE_09189 | chr1:154398672-154408855 | CD14 | | SE_16173 | chr1:154399945-154400671 | CD4_Naive_Primary_7pool | | SE_18405 | chr1:154399517-154407766 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19165 | chr1:154401205-154402489 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_24531 | chr1:154399580-154400359 | Colon_Crypt_2 | | SE_26130 | chr1:154399302-154401704 | Duodenum_Smooth_Muscle | | SE_26877 | chr1:154399516-154400662 | Esophagus | | SE_26877 | chr1:154400694-154402391 | Esophagus | | SE_32086 | chr1:154399571-154400607 | Gastric | | SE_32086 | chr1:154400656-154401897 | Gastric | | SE_41139 | chr1:154399325-154402156 | Left_Ventricle | | SE_41647 | chr1:154399531-154400535 | LNCaP | | SE_41647 | chr1:154400745-154403911 | LNCaP | | SE_42431 | chr1:154399355-154400656 | Lung | | SE_42431 | chr1:154400696-154402137 | Lung | | SE_47983 | chr1:154399591-154400258 | Pancreas | | SE_47983 | chr1:154400922-154401243 | Pancreas | | SE_48261 | chr1:154399318-154401864 | Psoas_Muscle | | SE_48934 | chr1:154399344-154402194 | Right_Atrium | | SE_50453 | chr1:154399516-154401315 | Sigmoid_Colon | | SE_51380 | chr1:154399138-154401914 | Skeletal_Muscle | | SE_52880 | chr1:154399518-154401631 | Small_Intestine | | SE_54618 | chr1:154399097-154409137 | Stomach_Smooth_Muscle | | SE_62668 | chr1:154357227-154415486 | Tonsil | | SE_65390 | chr1:154399323-154400849 | Pancreatic_islets | | SE_65390 | chr1:154400868-154402476 | Pancreatic_islets |
|
| | 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 |
| GH01I154427 | chr1 | 154399576 | 154401508 |
|
Enhancer Sequence | AGGGCAGGTC TCTGGGATGC CTGACTGTGT CTTCCTTGCC AGTGCCTGGC TGCTGCAGCC 60
TCCTCAAATG TTTATCAAAC ACAGGACTTG CCCACCGTGG GAGAAAGTAA GGCCATAGGT 120
GTCTCAGGAA CCTGCCCAAA CTCGCCTGGC TGCACGGTGA CAATTCAACC AGCTTTCTTA 180
CCCAAGGTCT GTTGGTGACC AGAGAAAACC TTAGATGACC GGCTGCCATG ATGGCCTTAT 240
ATCTGTCCCT TTTCTGCCAG CCTTGAGGTA GAGGGTGCCA GGGAGGAGGA CTCTGGCTCT 300
AGGTGTTAAA GTGAGAGGGA AGTGTGAAGG GTATCTGTAT AGCTAGACAG GGCTCAATGC 360
CAGGCAGAGC TGTCTCCGCC CCTTTGATGT CTATGTCTCT GTCCCTGGAC TGTGGCCAGT 420
AGCCAGTGTG GACTCCAACC TCACCAGCTT TAGGGGTGTT ATCTGCCTGG GAGTCACTGA 480
TCCTTACTCC CTCCTCTGAC AGCCACCTTG GATGGGGTGA AAGGAAGGAC AGCCTGCCAA 540
GTATGAGATA AAAACGCCTC ATAAACAAGA AGGGATTTGC AGGCCAGGCA GAGAGCCTTG 600
TGCTGCTTCT GAGTCCCAGG AGCATGGGCG AGGAGGTGAG GTCAGGCACT CAGCAGCTGC 660
TGGTCCTCTC TGAAATCTTT GGCCAGATTT ATTGCTACTG CTTGCTAATA AATGGTTATG 720
CATTTGGTTC AAAGGACCAA GTGTGCTTAC ATGAAAACTG GCTGTGTTCC CTGGCCTCTG 780
TTTCCTTAGC TGGTTGGACT AATTTGATTG GTTAATAAAT GAGTCCAAGG TGGTTGGGCT 840
AATTTTTATC TTAGATTCTA TGACTCTATA ACTGCTACTC AAAAAAAGTG TACTTGTTCC 900
TTTAATCTTT AATCTTATTT TTCTTGAGTA GTAGAATACA CCCAATTTTT TTCAAGGGGT 960
AGAGAATGCA TTTTTTTTTT AACCTTCCAG TTTGGTCCCT AGAGTAAACA CAGCATTGCT 1020
GTAGTAGATG TAGGGTACTG GAGGGAGCAT GGAACAGGGA ACCAGAAGCC CTGGTTCCTA 1080
CCCCAGCTGG GCATCTGGGC CAGTCTCTTG ATTCCTCTGT GCCTCAGTTA CCAACTATAT 1140
AACGGGCATT CTGCCATGAA TACCCTGCGA TTTGGAAACC TCCTGTGTAC GTGTGCACTT 1200
GGGTGCCTGG CATTCATTCC TAATGGCATC CATTCGTTCA CACATTCATC CAGTACTCAG 1260
CAGACTCCTG CCATGGGCCA GGCAACGTCC CGGGCACTTG GAATATAATG GAGAACAAAG 1320
CAGGGTGCCT ACTTCTGTGG TGCTTGGAGT CTTGAGGGGA AGAGAGACAC GGAATTCGTA 1380
ATTACATGGC AGCGTGTGGG TGACGTATTG CAGAATGAGG GCCTAGTGGA GCTGGGGGAC 1440
CGGAAACGAT GTTTAGGCCG AGACCTGGAA TAGGAGGAGT TGTCGTGGGG ATGATGTAGG 1500
AAGAACGAGT GTGAGGAGGA GAGCGAGGGG AGTTGAGGGG AGGGCTCCAC ACCTTCTAAG 1560
GAGTGGGGAG AGATGAGGCC TCCAAGGACA GAAGGGCCCT GCAGGCCACG CTGAGGAGCT 1620
TGGACTTCAT CTTGTGGATG GTGGCAGGCC CTTGAAGGGT TTTCTAATCC AGGGAGTGGG 1680
GTGGCTGGAT CATGGCTTCA GAAGGCTCTC CCAGGCAGCT GGATGGTGAA GACCAGGTTG 1740
GGGAGGTCAC CAGGAGAATG CTGCCCTAAT CCAGGCAGAG GTGACGGTAG CCTGGGCCAC 1800
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