EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-11663 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr5:131820190-131821350 
Target genes
Number: 11             
NameEnsembl ID
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata1MA0035.3chr5:131820539-131820550AGAGATAAGGA-6.02
Sox3MA0514.1chr5:131820491-131820501AAAACAAAGG-6.02
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00037chr5:131820679-131837440Adipose_Nuclei
SE_06435chr5:131820979-131828153Brain_Hippocampus_Middle
SE_09163chr5:131820716-131828938CD14
SE_10340chr5:131821077-131828016CD19_Primary
SE_10915chr5:131818633-131838738CD20
SE_11856chr5:131819920-131820627CD3
SE_11856chr5:131820867-131826566CD3
SE_13479chr5:131818971-131820466CD34_Primary_RO01536
SE_13479chr5:131820821-131827719CD34_Primary_RO01536
SE_14495chr5:131821083-131828600CD4_Memory_Primary_7pool
SE_15423chr5:131820763-131822653CD4_Memory_Primary_8pool
SE_16894chr5:131821079-131828658CD4p_CD225int_CD127p_Tmem
SE_17370chr5:131818848-131837330CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131818558-131837415CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131818792-131837424CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131818869-131820748CD4p_CD25-_Il17p_PMAstim_Th17
SE_19103chr5:131820789-131828689CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131818509-131828458CD56
SE_21523chr5:131820966-131828488CD8_Naive_7pool
SE_21960chr5:131821153-131828292CD8_Naive_8pool
SE_22284chr5:131818534-131837164CD8_primiary
SE_25340chr5:131818854-131820708DND41
SE_25340chr5:131820753-131827693DND41
SE_25784chr5:131820891-131828422Duodenum_Smooth_Muscle
SE_27629chr5:131820802-131827931Fetal_Intestine
SE_31393chr5:131819213-131820433Gastric
SE_31393chr5:131821009-131824351Gastric
SE_40726chr5:131820985-131824375Left_Ventricle
SE_42103chr5:131818931-131820682Lung
SE_42103chr5:131820940-131824330Lung
SE_50051chr5:131818807-131820703Sigmoid_Colon
SE_50051chr5:131820849-131828484Sigmoid_Colon
SE_52336chr5:131818890-131820627Small_Intestine
SE_52336chr5:131820826-131828467Small_Intestine
SE_53285chr5:131819536-131820579Spleen
SE_53285chr5:131820823-131828357Spleen
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131820932-131822102Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5131820274131820350
Number: 1             
IDChromosomeStartEnd
GH05I132485chr5131820281131820430
Enhancer Sequence
TGGGGACAGA AGAGCAAGAG GCTATCAACT CCCTTCCAGT GCAGACTCAC CCTGTGGCCC 60
TGCCCTCAAT GAGCCAGCTC CTCTCAGCCA GTATCACACC CTTGGCCATT TTCACAATCT 120
CAGATAGGAT GCAGAAGTGC ACTGCAGTCA GGACAAGGGC CCGGGAGGGA GGAGGCAGAA 180
ATGCATGTTG GCACTGGTCC TCAATTCATT TTCCCACCCC TCTCACACCC ACTCTCTGGT 240
ATAGCATCTC CACGACTTCC CTCTCAACTG TGTAAGGACA TAGTAAGAGG GAATGTGGCT 300
TAAAACAAAG GTTAGCATAA TAAATCAAGA AAAGATGACT AGAAAAGCTA GAGATAAGGA 360
ACGACATCCA TGTCTCAATT TTTTGGGCTA ATGGAACAGC TGGCGTACAA CTACTGCAAA 420
AACTTTTTTT TGAAATGGAG TTTTGCTCTT GTTGCCCAGG CTGGAGTGCA ATGACACAAT 480
CTCAGCTCAC TGCAACCTCC GCCTCTCAGG TTCAAGCGAT TCTCCTGCCT CAGCCTTCAG 540
AGTAGCTGGG ATTACAGGCA TGCGCCACCA GGCCCAGCTA ATTTTTATAT TTTTGGTAGA 600
GATGGGTTTC ACCATGTTAG TCAGGCTGGT CTCAAACTCC TGACCTCAGG TGATCCACCC 660
ACCTTCGCCT TCCAAAGTGC TGGGATTACA GGCATGAGCC ACTGCCCCCG GCTGCAAAAA 720
CTATATTCAC TTTCAAAACT GAAGCAGAAA AAAAAACCTG GAGGATAATT TGCTAACTTT 780
TTCTATAAAG CCATCATCAT ATTAACGGAT CCTAAAGGCT GATTATTGAA GCCTGATGTG 840
CATTTCCCGA ACTAGCAGGG CTGGGGCATG TTGGGGCAGA GGATGCAGGC CAGGGACCCA 900
TCGCTGATAG TGCCTGACTC ACAGAGCTGT CTGATGCCCC AAGGCTTGCT TCAGGACGGC 960
CTGTCAGAGG CCAGGCCTCC CACCTGCCTT CCCTTCCCAT GGTGGCTTTC CCACCAGTCA 1020
AGCCACGTGA ATGTGGCACT TGTGGGACAA TGCAAGCAGC CAGGTGACAA CAGCAGCTAC 1080
CCATCCTCTG ATTTGGAAGC TTCACTGGTT CTCTCTCCTC ACTGAGAAAC GGTCACTTCA 1140
AGAGTGCCCA GGTAGGAAGG 1160