EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS048-03157 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr1:204386170-204387620 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:204386205-204386223GGAAGGAAGGGAGGGAAA+6.42
EWSR1-FLI1MA0149.1chr1:204386197-204386215AGAGAGAAGGAAGGAAGG+6.71
EWSR1-FLI1MA0149.1chr1:204386201-204386219AGAAGGAAGGAAGGGAGG+7.79
ZNF263MA0528.1chr1:204386181-204386202AGGGGAGAGGGAGGGGAGAGA+6.01
ZNF263MA0528.1chr1:204386183-204386204GGGAGAGGGAGGGGAGAGAGA+6.18
ZNF263MA0528.1chr1:204386206-204386227GAAGGAAGGGAGGGAAAAGAA+6.28
ZNF263MA0528.1chr1:204386199-204386220AGAGAAGGAAGGAAGGGAGGG+6.7
ZNF263MA0528.1chr1:204386202-204386223GAAGGAAGGAAGGGAGGGAAA+6.8
ZNF263MA0528.1chr1:204386176-204386197GGGGGAGGGGAGAGGGAGGGG+7.05
ZNF263MA0528.1chr1:204386187-204386208GAGGGAGGGGAGAGAGAAGGA+7.15
Number of super-enhancer constituents: 19             
IDCoordinateTissue/cell
SE_00064chr1:204384866-204397800Adipose_Nuclei
SE_07775chr1:204386029-204387635Brain_Inferior_Temporal_Lobe
SE_13620chr1:204385766-204387113CD34_Primary_RO01536
SE_14222chr1:204386046-204387079CD34_Primary_RO01549
SE_14854chr1:204385835-204387334CD4_Memory_Primary_7pool
SE_18998chr1:204385972-204387371CD4p_CD25-_Il17-_PMAstim_Th
SE_20531chr1:204386029-204387877CD56
SE_23499chr1:204386155-204387617Colon_Crypt_1
SE_26359chr1:204385194-204389873Duodenum_Smooth_Muscle
SE_26688chr1:204386007-204388336Esophagus
SE_28866chr1:204385237-204387899Fetal_Intestine_Large
SE_32169chr1:204386018-204387890Gastric
SE_34711chr1:204384952-204393525HeLa
SE_36671chr1:204386118-204388767HMEC
SE_40776chr1:204386109-204388741Left_Ventricle
SE_42225chr1:204386065-204387844Lung
SE_45371chr1:204385950-204387716NHLF
SE_48201chr1:204386214-204387082Psoas_Muscle
SE_64411chr1:204386123-204388806NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1204386444204387188
Number: 1             
IDChromosomeStartEnd
GH01I204415chr1204384804204390490
Enhancer Sequence
AGTGTGGGGG GAGGGGAGAG GGAGGGGAGA GAGAAGGAAG GAAGGGAGGG AAAAGAAAGA 60
AAGAACCTGA GCAACAGTCT ACAAAAGTTT ATGGAAAAAA AAAGTTTAAA AAATTAAAAT 120
ATTTGAGAGC TGCCTCTGAG AATATGTGAC TTTGCCTTGT TCGTCTCAGC TGGAAAAGTG 180
TGACTCAGCC TTCCCAAGCC TGCTAGAGGG CAGAGGGAGG CCAGATCTGT ACACAGAGAT 240
AACATGTTGC CAAGGCCGTG TGCAAGCTGG TGAAGACAAA AAGTCCTTCC ATTGGCAAGC 300
TGACTGGCAC TTTGGCCGGA GAAAATTAAA ACCTCAGTTA ATTCTGTTTA TTTTAAAAGA 360
CTTTGCCAGA CTGAGGTAAA GGGTATATGG CTCTTGATTT TTTCGGAGTC ACCACCAGCT 420
CCAAAATCTG ATATCGCAGT ATCTCCCACT CTGGCTGCCG CCTCCTACCA ATCCACACTG 480
CCCTGATAAC CCTATTCAGC TGCTGGTTAA CTCCTCAGAG ACCACAAACC ATTGCTCTTA 540
CCACTTTTTG TGATCCATCA CACTCTTCAT TTCCCTCCTT ACTCAGCATG AATTTCCATG 600
ATCCAGTATT AAAACTACCC CCTTGCCCTT CTACTCCCTG GCAAAACTCC AACCCTAGTT 660
AAACCCAACT ACTCACGCAT TCTGCGCCTG CACCCTTGCA GCTAATCATT GCTTAAGAAG 720
ATCGCTCAGA CATGCTGAGT GACTCACTTC ATACTTGTGA TCACAATCTC ATCGACACCA 780
GGCACTCCCA CCACAGTTCC CTAGAAGCTT TGCTTCTCCT ACACTCTGAG ACTGTCTCAC 840
AATACTTCTT TCTTCAAATT TCCAGCATTT CCCATAAACA CACATTCTCA GTTTATGATC 900
ACACTCATAC TTCAAGAAAA AACAGATACA ACTGGACATA AATCACCTCA TCTTTCCCTG 960
AACAAATCCA CCGGCATCTG GACCCACATA ATCTGCCTTC AATCCTGCCA CAACCCAAGA 1020
AACCTCCTGG ATGCCATCCC TCCATTTTCA CTTAAGGAAT TCTGACCTCT CTTATCCCTT 1080
CTCCCTAGTA ACATACACGT TTCTCTCACT AATAGATCAT TCACATTTAC ATAACTTAAT 1140
ATCAGCTATA TTAAAAATAA AAAGACCACC CAGCATGGTG GCTTACGCCT GTAATCCCTA 1200
CACTTTGCAG GGCCAAGGCA GGGGGCTTGA GCCAAGGCTT GAGCCCAAGT GTTCAAGACC 1260
AGCCTGGACG ACATAGCAAG ACCTTGTCTC TACAAAAATT TAAAAAATTC GCTGGGCGTG 1320
GTGGCTCACA CCTGTAGTCC CAGCTACTCA GGAGGTTGAG GTGGGAGGAC TGCTTGAGCC 1380
AACGAGGTTA GGGCTGCAGT GAGCCAAGAA CACACCACCA CCCTGCAGCC TGGGTGACAG 1440
AGCAAGACTC 1450