EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS177-13442 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr2:238610920-238612040 
Target genes
Number: 7             
NameEnsembl ID
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
DUX4MA0468.1chr2:238611762-238611773TAATCTAATCA+6.32
EWSR1-FLI1MA0149.1chr2:238611288-238611306ATTTCCTTCCTTCTTTTC-6.43
EWSR1-FLI1MA0149.1chr2:238611292-238611310CCTTCCTTCTTTTCTTTC-7.01
SP2MA0516.2chr2:238611424-238611441CAGGGGGAGGGGCTTGT-6.28
Number of super-enhancer constituents: 58             
IDCoordinateTissue/cell
SE_00318chr2:238608341-238613202Adipose_Nuclei
SE_01566chr2:238608239-238612909Aorta
SE_02327chr2:238610486-238613462Astrocytes
SE_03013chr2:238611678-238612456Bladder
SE_09199chr2:238608075-238617357CD14
SE_11030chr2:238594416-238614117CD20
SE_11900chr2:238610779-238611561CD3
SE_12920chr2:238610056-238611071CD34_Primary_RO01480
SE_13435chr2:238608412-238612777CD34_Primary_RO01536
SE_14109chr2:238610465-238612214CD34_Primary_RO01549
SE_14422chr2:238608296-238612923CD4_Memory_Primary_7pool
SE_15836chr2:238610543-238612027CD4_Naive_Primary_7pool
SE_16319chr2:238610869-238612150CD4_Naive_Primary_8pool
SE_16886chr2:238608443-238612125CD4p_CD225int_CD127p_Tmem
SE_17380chr2:238594947-238612837CD4p_CD25-_CD45RAp_Naive
SE_17823chr2:238594491-238617199CD4p_CD25-_CD45ROp_Memory
SE_18373chr2:238600747-238613962CD4p_CD25-_Il17-_PMAstim_Th
SE_19179chr2:238608152-238616656CD4p_CD25-_Il17p_PMAstim_Th17
SE_20077chr2:238608252-238612480CD56
SE_20788chr2:238608577-238612222CD8_Memory_7pool
SE_21974chr2:238610814-238612335CD8_Naive_8pool
SE_22424chr2:238599282-238612396CD8_primiary
SE_23331chr2:238610605-238612614Colon_Crypt_1
SE_23963chr2:238611320-238611502Colon_Crypt_2
SE_23963chr2:238611555-238611871Colon_Crypt_2
SE_25815chr2:238608299-238618181Duodenum_Smooth_Muscle
SE_26722chr2:238608218-238612884Esophagus
SE_28399chr2:238610630-238612358Fetal_Intestine
SE_29463chr2:238610591-238612509Fetal_Intestine_Large
SE_29646chr2:238608292-238612938Fetal_Muscle
SE_31908chr2:238608424-238612885Gastric
SE_36086chr2:238610778-238613929HMEC
SE_36919chr2:238608262-238615293HSMMtube
SE_38133chr2:238608238-238614216HUVEC
SE_40633chr2:238608186-238614216Left_Ventricle
SE_42111chr2:238608226-238618523Lung
SE_43921chr2:238608281-238613700MM1S
SE_44921chr2:238610446-238612852NHLF
SE_45786chr2:238608313-238614636Osteoblasts
SE_48071chr2:238608183-238612914Psoas_Muscle
SE_48757chr2:238608327-238612910Right_Atrium
SE_49604chr2:238611354-238612802Right_Ventricle
SE_50280chr2:238608222-238612914Sigmoid_Colon
SE_51094chr2:238608086-238615331Skeletal_Muscle
SE_51777chr2:238610510-238614092Skeletal_Muscle_Myoblast
SE_52590chr2:238608351-238612899Small_Intestine
SE_53427chr2:238608194-238612891Spleen
SE_54582chr2:238608047-238614343Stomach_Smooth_Muscle
SE_55444chr2:238610870-238611260Thymus
SE_55444chr2:238611282-238612125Thymus
SE_58523chr2:238563966-238621920Ly1
SE_59868chr2:238570692-238624050Ly4
SE_62022chr2:238577134-238613107Toledo
SE_62653chr2:238581155-238612908Tonsil
SE_63565chr2:238610411-238614143HSMM
SE_64519chr2:238611381-238612168NHEK
SE_65656chr2:238607949-238613154Pancreatic_islets
SE_67420chr2:238608281-238613700MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2238611190238611575
Number: 1             
IDChromosomeStartEnd
GH02I237699chr2238608260238614656
Enhancer Sequence
AGGCAACTTT GATAGTAAAT GGAATCTTTT TTTCCCAGCC ATCCCCACCC TCAAAGAGTA 60
TCTTGCTGTA AGACCTAGTT CCTGTAAAAC TCTGTCTGTG GGGTCCCTGG CCAGGATGGG 120
TGGGATCCCA GGGAAAGGGC CAGGCTGTGT GTTCTGAACA GGAATGGTTC TGGACCAACC 180
ATTGTGGGCA TTCCTGAGAA GCCAGGGAGC CTGGATCTTG TCAGAGGAGC TCCTCCCTCT 240
GCTCCATCCT AACCCCGCGG GCAGCAGCAG GAACTGAGAG AGGACACGGT GGGGGCAGCG 300
CTGCAAAACC CAGCAGCGGG CCACCTTCCA GCAGCAGAAA GCATGAGTTT TGGTTTTGGG 360
GCTCTTCCAT TTCCTTCCTT CTTTTCTTTC TTTTTAAATT TTTGCTCTTT GTTATGAAAC 420
AGCAGCCAGA CCGAGCTATG CATGTCCTGC TGCACGGCAG GGGCCCTTAT CTTGAACGAC 480
TCCACATACT GGGCAAGGAG GTGGCAGGGG GAGGGGCTTG TGGGAACCCA GATCTGGGAT 540
GGGACTCAGC CAACAGTTTA AAGAGCCCTG TGCCCCCACT ACCCAGCCTC AACAATTGTT 600
AGCTTATAGC CGTTTACACC CCACCCAGGT TATTTGAAGA CAAGTCAGAG GGAGATAATT 660
TCACTGTACT CCTAAATGTT TTAGTATCTC AGCAAAGATT GTATGGGCAG AGAAAGGAGG 720
CTTCAGGGTG TAGGACCCCA GGAGCAGGCA AGGGCTTGCT CTTTCCCTGT TGGCTCCTGT 780
AGGGTGGGGA CAGACCAGCC CCCATGAACC CTAGCGAGGG CCATGCCAAG AAGCCGCTGT 840
TCTAATCTAA TCAGTGGAGG ATCCAGCAAG CTCGGATGGG AGGGAAAGAA TGACTCAACC 900
TGCAGGCCGT CTGGGGTATG CACAGTCTCG TCTCCTGAGT TCTCTGAAGC CCTTTGCAGT 960
TTTTGCTTTG TATCCTAAAC TCCACAGGCC CGAACCCTGG CACTGAGCTT GATCCGCTGC 1020
AGCCCAGCCC GTTCCTGTCC CCATGCTGGA AGCAGCCTGT CAACTCACTT CCTTGGTTTC 1080
CTGTTGCTCT TCCCACCCCA TACCTGCTCC CCACATTTCT 1120