EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS049-06331 
Organism
Homo sapiens 
Tissue/cell
Fetal_spinal_cord 
Coordinate
chr5:139014830-139016530 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZfxMA0146.2chr5:139015473-139015487TGGGCCCAGGCCTG+6.06
Number of super-enhancer constituents: 57             
IDCoordinateTissue/cell
SE_00187chr5:139014509-139019352Adipose_Nuclei
SE_03140chr5:139015579-139017003Brain_Angular_Gyrus
SE_03865chr5:139013764-139020195Brain_Anterior_Caudate
SE_04768chr5:139014383-139019998Brain_Cingulate_Gyrus
SE_05771chr5:139011730-139020155Brain_Hippocampus_Middle
SE_06683chr5:139015040-139019199Brain_Hippocampus_Middle_150
SE_07722chr5:139012918-139019513Brain_Inferior_Temporal_Lobe
SE_08785chr5:139015511-139015888Brain_Mid_Frontal_Lobe
SE_10432chr5:139013248-139019966CD19_Primary
SE_11063chr5:139012685-139020525CD20
SE_13414chr5:139015146-139018531CD34_Primary_RO01536
SE_15340chr5:139015089-139018977CD4_Memory_Primary_7pool
SE_20188chr5:139013581-139019539CD56
SE_21110chr5:139014397-139018750CD8_Memory_7pool
SE_23515chr5:139014678-139020080Colon_Crypt_1
SE_24043chr5:139014785-139016516Colon_Crypt_2
SE_25255chr5:139015699-139018859Colon_Crypt_3
SE_26221chr5:139015059-139016998Duodenum_Smooth_Muscle
SE_26778chr5:139014734-139019107Esophagus
SE_27739chr5:139014873-139019521Fetal_Intestine
SE_28684chr5:139014822-139019411Fetal_Intestine_Large
SE_29581chr5:139014722-139021564Fetal_Muscle
SE_30930chr5:139013570-139018802Fetal_Thymus
SE_31417chr5:139014669-139019242Gastric
SE_32616chr5:139013641-139019077GM12878
SE_33677chr5:139015391-139020504H2171
SE_34346chr5:139014559-139018989HCT-116
SE_36941chr5:139014574-139020500HSMMtube
SE_39957chr5:139015441-139018920K562
SE_40649chr5:139014699-139019130Left_Ventricle
SE_42197chr5:139014590-139018940Lung
SE_43428chr5:139014665-139017028MCF-7
SE_44620chr5:139014761-139018757NHDF-Ad
SE_45282chr5:139015499-139018604NHLF
SE_45813chr5:139015155-139018836Osteoblasts
SE_47229chr5:139015018-139018698Panc1
SE_47460chr5:139014931-139016612Pancreas
SE_48055chr5:139014610-139023286Psoas_Muscle
SE_48579chr5:139014693-139019167Right_Atrium
SE_50216chr5:139014115-139019780Sigmoid_Colon
SE_51090chr5:139014641-139023789Skeletal_Muscle
SE_51845chr5:139015451-139016230Skeletal_Muscle_Myoblast
SE_52795chr5:139014617-139019623Small_Intestine
SE_53351chr5:139013628-139018944Spleen
SE_55117chr5:139014850-139018076Thymus
SE_55730chr5:139014808-139020111u87
SE_56812chr5:139015490-139016200VACO_400
SE_58504chr5:139012442-139092243Ly1
SE_58973chr5:139014489-139051808Ly3
SE_59917chr5:139013000-139054281Ly4
SE_60524chr5:139012854-139052007DHL6
SE_61337chr5:139014342-139051822HBL1
SE_62370chr5:139013548-139054462Tonsil
SE_63555chr5:139015451-139018883HSMM
SE_65250chr5:139014796-139021014Pancreatic_islets
SE_67548chr5:139014808-139020111u87
SE_68692chr5:139015307-139016259H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5139015811139016118
Enhancer Sequence
TGCCCTCCTT TGAGCTGGGC TAGCTCCTGG GACATCCAGG GACCTGGGGA AGACTGGCTG 60
GGCCCTTTTG CAGCCTATGG CTCACATGCC CACTTGTTAA GGCCTGCAAG AGTGTGCCCA 120
CAAACAGGGT GAGCAGGCAG AATAATGGCC ATGGCTAGCC AGACTGTGTG TCCTTGCCCA 180
GTGTCTGTCT GTCCTTCCCC TTACCTTGGG GGACAAAAGG GAATCCAGTT GTCCTGCCTG 240
GTGAATAAAA GCCTGGGGTT GGGGGAGGAT TTGCCTCCAG CCACGGAGGA GGGGTATGCT 300
GTGGAAGGAG GCCAGATCTC CCCCAGCTGT TTCCCAGCTC TGTTTGAAGG GGAAGGGAGA 360
GGGATAAATG ACTGGGTGAT TGTGGCACCT ACAGCCAGCA TCTTTCCTCT CCACATTCTA 420
GGTCACAGGC CCACACCTCT CTCCCTAGTC AAAGAGAGCC TCTGTGAGGG GGTTGAAGGG 480
TGTCTTGGAT CTGTGGGCAG GACTTGGGAT CTGGGCACAG AGAGGTTGGG GAATTAACAA 540
AGGTCACACA GCCAGGCAAA ACTAGGGAAT GTGGGGAGTC ATTCTAGACA GGACCTTTAG 600
GGGGAGCTCC CTGGCTACAA GAGATTTCCT GGAAGCCCTT GGGTGGGCCC AGGCCTGAAC 660
TGAGGAAGTG AGGGCTACAG CCCAGCTGGC CTTGCACTGG AACCACAGGA GTGGCCTTTA 720
AGGGTGTGCT GAAGGACTGA TGAATCTTGG CCCTGTTCCC ACACACATGC ACCACTGGGA 780
ATGGGAGTGG GGAGATTGCT GAGCTCTGGG GCCAGCCCTG TTTCCTGCTT TGGATTTGGA 840
ATGGGGAGAG CCTTTCTGGG GACTGAAACT GGTGCTTCAG CTTCTCTAGG GGGAAATGGA 900
GAAATGGAAA GGGGGACTGA CAAGGGATAG TCCTTAAGGA GTTTATTTGG GAGGCTCTGG 960
GTCCCTTTGT AACTAGGTGG GTGACCTTTA GGAGGGAAGT GCTTTGTGTT CTACAGCTTT 1020
CTGAGAGTGG CAGGAAATGG GGCCAGTAGC AGTGCACACT AGTTGGGTTG CACCTGGTGA 1080
GAGATTAGGG GTGGTTTCCC CACCAAGGTC TCTGAGCCAG AGCTTTCAGC TGCATGAGCA 1140
CAGCCTGCTC CCCCTGTGGA GGGGATTCTG GGGTGGGTGT GGTTGTATAC TGGGGGAAGT 1200
GAGAATGTGG CCTCTCTGTG GGTGAGTGCA GCACCGTGAA TTGTGTTTGT AACACTTGAG 1260
TTGTGTTTCC CAGGTGTATG TGATGGCAGA ACTAGTTTTG CTGCTGGGGT GAATCAGGTT 1320
CCTGGAAGGG ACTGGACTAA CATGGAGAGA ATGATGCTAA GTAGTTACAG TCATTATTAT 1380
ATACACATGA CTTAGTAGTA TAGAACCATT AGCAATGACC AAGACCACCT GTGTGTCGAG 1440
TGCTTACCAT GTGCCTGGTG CTGTGCTAAG CACCTCACCT GCAGTGGCTC ATTTAGTCCT 1500
GTCAGAACCC TGCAAGTTCA TGCTGGTTTG CCTGGTGTTT GTTTATTGTG CCATGTTGGG 1560
TGGGGTATAA TTTTATTCAA GTTGGAAGAT GCAAAACAGC TTTATCCCTC TCTTAGTTAC 1620
TGGGGTGCAA CTTATGGCAG CATTTGCCCC TGTCATATTC TATACTTGGG CTCCTGGTCC 1680
CATCCTTTTG CCAGTATGGG 1700