EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-57045 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr9:33150790-33152160 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1328899chr933151415hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:33150982-33151000GGAAGGAAATAAGTAAGG+6.5
EWSR1-FLI1MA0149.1chr9:33150978-33150996GGAAGGAAGGAAATAAGT+6.7
EWSR1-FLI1MA0149.1chr9:33150962-33150980GGATGGAAAGAAGGAAGG+7.73
EWSR1-FLI1MA0149.1chr9:33150974-33150992GGAAGGAAGGAAGGAAAT+9.03
EWSR1-FLI1MA0149.1chr9:33150970-33150988AGAAGGAAGGAAGGAAGG+9.09
EWSR1-FLI1MA0149.1chr9:33150966-33150984GGAAAGAAGGAAGGAAGG+9.47
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00330chr9:33150154-33152533Adipose_Nuclei
SE_00992chr9:33150845-33151621Adrenal_Gland
SE_03080chr9:33150830-33151209Bladder
SE_09459chr9:33150683-33152077CD14
SE_10229chr9:33150691-33152191CD19_Primary
SE_10912chr9:33119344-33169982CD20
SE_19329chr9:33150695-33152114CD4p_CD25-_Il17p_PMAstim_Th17
SE_20045chr9:33150690-33152312CD56
SE_22416chr9:33150710-33152253CD8_primiary
SE_23687chr9:33150875-33151683Colon_Crypt_1
SE_26031chr9:33150287-33152385Duodenum_Smooth_Muscle
SE_26859chr9:33150779-33151670Esophagus
SE_27770chr9:33149455-33152321Fetal_Intestine
SE_28724chr9:33149325-33152320Fetal_Intestine_Large
SE_29800chr9:33150488-33152194Fetal_Muscle
SE_31534chr9:33150777-33151683Gastric
SE_34775chr9:33150487-33152230HeLa
SE_40894chr9:33150769-33152080Left_Ventricle
SE_41831chr9:33150862-33151334LNCaP
SE_42236chr9:33150804-33151823Lung
SE_44340chr9:33150635-33152125NHDF-Ad
SE_45447chr9:33150452-33151912NHLF
SE_45731chr9:33149399-33152178Osteoblasts
SE_46917chr9:33150883-33151589Ovary
SE_47814chr9:33151298-33151559Pancreas
SE_48426chr9:33150761-33152145Psoas_Muscle
SE_48738chr9:33150773-33151797Right_Atrium
SE_50176chr9:33150800-33151701Sigmoid_Colon
SE_51651chr9:33149245-33152315Skeletal_Muscle
SE_52621chr9:33150782-33151822Small_Intestine
SE_53402chr9:33150804-33151863Spleen
SE_56627chr9:33150139-33152742u87
SE_58985chr9:33124740-33168862Ly3
SE_62118chr9:33106994-33169093Toledo
SE_62346chr9:33106942-33169226Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr93315093633151964
chr93315082833152043
Number: 1             
IDChromosomeStartEnd
GH09I033149chr93314900333152397
Enhancer Sequence
GGCAAGAGCA AAAACAGATA CACAAACTAT AAATACGTTA GAATAGTTGC CTGTGATATA 60
CCTGGGAAAT AGAAGTGGGA ATGAGGACAA AATAAAACAA ATACATGAGG CAAGAGAGTC 120
CATGAGTAGA CCCCAATGAT GATTATTGGC CATGAAAGGA AGCTTGATGG CTGGATGGAA 180
AGAAGGAAGG AAGGAAGGAA ATAAGTAAGG GAGAGATGGC GGATGGAGCT GGATGTGTCC 240
TTCCAGGGCT GTACAAAGGA GGGGGACCCC AACCCCTAGT CCAGACAAAG GTCCCTAAGG 300
CAGGTGTACA GTATTGTGGG GATGAATTCA TCAGCCACGA GAGACTGACC CATCTAATGT 360
TAAATTCACT TCCCTGCTCT GACTGCTGAC TCACCAGCAG TTAGCTTATC CTGCGGCTTC 420
CCTTGCAGTG AATTCAGCCA GAGATTTCTA AGCTACTCAA TAACAGTTCT AATCTTCCCA 480
GTAAAGCTGC AACTTTGCAT TCCAGTATGT AAGTAAGTCT CCTGGGAGTT TTATTACTGA 540
GTCAGCTGCC CCTCTAATCA GTTTTGGAGC CCCAGCAGAT TTTCTGGAGC TGCGGTGCTG 600
ACTACGAGCA CATCCTTCTC TCTCCACCTA GAACCAGACC TTGGACTGTG GAGGGCCCAC 660
TACTCCTATG GGCCATCTGG GCACTCAGCC AGCCAAGTAC TCCTGGCAAT ATCTCTCTGG 720
TGTCAGGACT ACTTTAAATG TAGCCAGCTC CAATTTCCTT CTCTAAGGAG TGGGGATAAT 780
TATGCCTTCC TTTCAGATGT AAGTGAAATA ATACATATAC ATACTTATCG CATGTTCTTA 840
TTGAGCTAAT AGATGTTCAA TAAATGTTAC TTTCCCTTCT CCCCTGACTC CTTAGAACTT 900
CAGAGCTTAC AAATTACTAC AGCTCTATCA GCACACATGG CTAAATTTTC ACATTTCTAC 960
TCTTAGCCAC TAGAATCACT GATAGATTTG GAGGAAAACT CTGGGACCTT AAAGGGTCCC 1020
TGGAGTATTA CATAAAGCTT CTTGCAGCAT GAGAGTTGAA CAGAAATTCT GTTCATCTTT 1080
TGCTGTCGAA GCCAAGTTGG TGGCTTCTAA AGAACCAACT TAGAAGAAAA CTCAGGAGAA 1140
AAATTTTATC ATTTTGGGAT GGTGAAGACC TGCTTAAGTA TGAAAGCAAC CTGAAGTCAT 1200
AAAGGAAAAC ATAGATTTAA ACACATAAAA ATTCAAAACT TCTGGCCGAG TGCAGTGGCT 1260
CACGCCTGTA ACCCCAGCAC TTTGGGAGGA TCATTTGAGA TCAGGAGTTT GAGATCAGCT 1320
TGACCTACAT AGTGAAACCC CGTCTCTACT AAAACACAAA AATTAGCTGG 1370